Canonical Allele Identifier: CA1437726

Gene: OBSCN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.228339984C>T , CM000663.2:g.228339984C>T	GRCh38
NC_000001.10:g.228527685C>T , CM000663.1:g.228527685C>T	GRCh37
NC_000001.9:g.226594308C>T	NCBI36
NG_032122.1:g.136825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284548.16:c.17298C>T	ENSP00000284548.11:p.Asp5766=
ENST00000570156.7:c.20169C>T	ENSP00000455507.2:p.Asp6723=
ENST00000636476.2:c.17301C>T	ENSP00000489816.2:p.Asp5767=
ENST00000662438.1:c.18843C>T	ENSP00000499633.1:p.Asp6281=
ENST00000664561.1:c.177C>T	ENSP00000499480.1:p.Asp59=
ENST00000664957.1:c.1220C>T
ENST00000680850.1:c.20169C>T MANE Select	ENSP00000505517.1:p.Asp6723=
ENST00000284548.15:c.17298C>T	ENSP00000284548.11:p.Asp5766=
ENST00000366707.8:c.20169C>T	ENSP00000355668.5:p.Asp6723=
ENST00000422127.5:c.17298C>T	ENSP00000409493.1:p.Asp5766=
ENST00000483539.2:c.4694-16834C>T
ENST00000570156.6:c.20169C>T	ENSP00000455507.2:p.Asp6723=
NM_001098623.2:c.17298C>T	NP_001092093.2:p.Asp5766=
NM_001271223.2:c.20169C>T	NP_001258152.2:p.Asp6723=
NM_052843.3:c.17298C>T	NP_443075.3:p.Asp5766=
XM_005273287.3:c.20472C>T	XP_005273344.1:p.Asp6824=
XM_005273288.3:c.20472C>T	XP_005273345.1:p.Asp6824=
XM_005273289.3:c.20469C>T	XP_005273346.1:p.Asp6823=
XM_005273290.3:c.20469C>T	XP_005273347.1:p.Asp6823=
XM_005273291.3:c.20436C>T	XP_005273348.1:p.Asp6812=
XM_005273292.3:c.20208C>T	XP_005273349.1:p.Asp6736=
XM_005273293.3:c.20208C>T	XP_005273350.1:p.Asp6736=
XM_005273294.3:c.20208C>T	XP_005273351.1:p.Asp6736=
XM_005273295.3:c.20196C>T	XP_005273352.1:p.Asp6732=
XM_005273296.3:c.20196C>T	XP_005273353.1:p.Asp6732=
XM_005273297.3:c.20196C>T	XP_005273354.1:p.Asp6732=
XM_005273298.3:c.20163C>T	XP_005273355.1:p.Asp6721=
XM_005273299.3:c.19944C>T	XP_005273356.1:p.Asp6648=
XM_005273300.3:c.19944C>T	XP_005273357.1:p.Asp6648=
XM_005273301.3:c.19944C>T	XP_005273358.1:p.Asp6648=
XM_005273302.3:c.19920C>T	XP_005273359.1:p.Asp6640=
XM_005273304.3:c.19680C>T	XP_005273361.1:p.Asp6560=
XM_005273305.3:c.19416C>T	XP_005273362.1:p.Asp6472=
XM_005273307.3:c.19350C>T	XP_005273364.1:p.Asp6450=
XM_005273309.3:c.20472C>T	XP_005273366.1:p.Asp6824=
XM_005273310.3:c.20469C>T	XP_005273367.1:p.Asp6823=
XM_006711819.2:c.20322C>T	XP_006711882.1:p.Asp6774=
XM_006711820.2:c.20208C>T	XP_006711883.1:p.Asp6736=
XM_006711821.2:c.19932C>T	XP_006711884.1:p.Asp6644=
XM_006711822.2:c.19896C>T	XP_006711885.1:p.Asp6632=
XM_006711823.2:c.19893C>T	XP_006711886.1:p.Asp6631=
XM_006711824.2:c.18888C>T	XP_006711887.1:p.Asp6296=
XM_006711825.2:c.17568C>T	XP_006711888.1:p.Asp5856=
XM_006711826.2:c.20472C>T	XP_006711889.1:p.Asp6824=
XM_006711827.2:c.18309C>T	XP_006711890.1:p.Asp6103=
XM_006711828.2:c.20169C>T	XP_006711891.1:p.Asp6723=
XM_006711829.2:c.18033C>T	XP_006711892.1:p.Asp6011=
XM_011544290.1:c.20196C>T	XP_011542592.1:p.Asp6732=
XM_011544291.1:c.19899C>T	XP_011542593.1:p.Asp6633=
XM_011544292.1:c.19680C>T	XP_011542594.1:p.Asp6560=
XM_011544293.1:c.19680C>T	XP_011542595.1:p.Asp6560=
XM_011544294.1:c.19680C>T	XP_011542596.1:p.Asp6560=
XM_011544295.1:c.19368C>T	XP_011542597.1:p.Asp6456=
XM_011544296.1:c.18624C>T	XP_011542598.1:p.Asp6208=
XM_011544297.1:c.18309C>T	XP_011542599.1:p.Asp6103=
XM_011544299.1:c.18033C>T	XP_011542601.1:p.Asp6011=
XM_005273287.5:c.20472C>T	XP_005273344.1:p.Asp6824=
XM_005273291.5:c.20436C>T	XP_005273348.1:p.Asp6812=
XM_005273298.5:c.20163C>T	XP_005273355.1:p.Asp6721=
XM_005273307.5:c.19350C>T	XP_005273364.1:p.Asp6450=
XM_006711822.4:c.19896C>T	XP_006711885.1:p.Asp6632=
XM_006711823.4:c.19893C>T	XP_006711886.1:p.Asp6631=
XM_006711827.4:c.18309C>T	XP_006711890.1:p.Asp6103=
XM_006711829.4:c.18033C>T	XP_006711892.1:p.Asp6011=
XM_011544297.3:c.18309C>T	XP_011542599.1:p.Asp6103=
XM_011544299.3:c.18033C>T	XP_011542601.1:p.Asp6011=
XM_017002443.2:c.20517C>T	XP_016857932.1:p.Asp6839=
XM_017002444.2:c.20517C>T	XP_016857933.1:p.Asp6839=
XM_017002445.2:c.20517C>T	XP_016857934.1:p.Asp6839=
XM_017002446.2:c.20514C>T	XP_016857935.1:p.Asp6838=
XM_017002447.2:c.20514C>T	XP_016857936.1:p.Asp6838=
XM_017002448.2:c.20367C>T	XP_016857937.1:p.Asp6789=
XM_017002449.2:c.20253C>T	XP_016857938.1:p.Asp6751=
XM_017002450.2:c.20253C>T	XP_016857939.1:p.Asp6751=
XM_017002451.2:c.20253C>T	XP_016857940.1:p.Asp6751=
XM_017002452.2:c.20253C>T	XP_016857941.1:p.Asp6751=
XM_017002453.2:c.20241C>T	XP_016857942.1:p.Asp6747=
XM_017002454.2:c.20241C>T	XP_016857943.1:p.Asp6747=
XM_017002455.2:c.20241C>T	XP_016857944.1:p.Asp6747=
XM_017002456.2:c.20241C>T	XP_016857945.1:p.Asp6747=
XM_017002457.2:c.20241C>T	XP_016857946.1:p.Asp6747=
XM_017002458.2:c.19989C>T	XP_016857947.1:p.Asp6663=
XM_017002459.2:c.19989C>T	XP_016857948.1:p.Asp6663=
XM_017002460.2:c.19989C>T	XP_016857949.1:p.Asp6663=
XM_017002461.2:c.19977C>T	XP_016857950.1:p.Asp6659=
XM_017002462.2:c.19965C>T	XP_016857951.1:p.Asp6655=
XM_017002463.2:c.19944C>T	XP_016857952.1:p.Asp6648=
XM_017002464.2:c.19893C>T	XP_016857953.1:p.Asp6631=
XM_017002465.2:c.19725C>T	XP_016857954.1:p.Asp6575=
XM_017002466.2:c.19725C>T	XP_016857955.1:p.Asp6575=
XM_017002467.2:c.19725C>T	XP_016857956.1:p.Asp6575=
XM_017002468.2:c.19461C>T	XP_016857957.1:p.Asp6487=
XM_017002469.2:c.18933C>T	XP_016857958.1:p.Asp6311=
XM_017002470.2:c.17613C>T	XP_016857959.1:p.Asp5871=
XM_017002471.2:c.20517C>T	XP_016857960.1:p.Asp6839=
XM_017002472.2:c.20514C>T	XP_016857961.1:p.Asp6838=
XM_017002473.2:c.20517C>T	XP_016857962.1:p.Asp6839=
NM_052843.4:c.17298C>T	NP_443075.3:p.Asp5766=
NM_001271223.3:c.20169C>T	NP_001258152.2:p.Asp6723=
NM_001386125.1:c.20169C>T MANE Select	NP_001373054.1:p.Asp6723=