Canonical Allele Identifier: CA423749145

Gene: OBSCN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.228316866T>G , CM000663.2:g.228316866T>G	GRCh38
NC_000001.10:g.228504567T>G , CM000663.1:g.228504567T>G	GRCh37
NC_000001.9:g.226571190T>G	NCBI36
NG_032122.1:g.113707T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284548.16:c.13443T>G	ENSP00000284548.11:p.Thr4481=
ENST00000570156.7:c.16314T>G	ENSP00000455507.2:p.Thr5438=
ENST00000636476.2:c.13443T>G	ENSP00000489816.2:p.Thr4481=
ENST00000662438.1:c.14988T>G	ENSP00000499633.1:p.Thr4996=
ENST00000680850.1:c.16314T>G MANE Select	ENSP00000505517.1:p.Thr5438=
ENST00000284548.15:c.13443T>G	ENSP00000284548.11:p.Thr4481=
ENST00000366707.8:c.16314T>G	ENSP00000355668.5:p.Thr5438=
ENST00000422127.5:c.13443T>G	ENSP00000409493.1:p.Thr4481=
ENST00000483539.2:c.4693+12413T>G
ENST00000570156.6:c.16314T>G	ENSP00000455507.2:p.Thr5438=
NM_001098623.2:c.13443T>G	NP_001092093.2:p.Thr4481=
NM_001271223.2:c.16314T>G	NP_001258152.2:p.Thr5438=
NM_052843.3:c.13443T>G	NP_443075.3:p.Thr4481=
XM_005273287.3:c.16614T>G	XP_005273344.1:p.Thr5538=
XM_005273288.3:c.16614T>G	XP_005273345.1:p.Thr5538=
XM_005273289.3:c.16614T>G	XP_005273346.1:p.Thr5538=
XM_005273290.3:c.16614T>G	XP_005273347.1:p.Thr5538=
XM_005273291.3:c.16578T>G	XP_005273348.1:p.Thr5526=
XM_005273292.3:c.16350T>G	XP_005273349.1:p.Thr5450=
XM_005273293.3:c.16350T>G	XP_005273350.1:p.Thr5450=
XM_005273294.3:c.16350T>G	XP_005273351.1:p.Thr5450=
XM_005273295.3:c.16338T>G	XP_005273352.1:p.Thr5446=
XM_005273296.3:c.16338T>G	XP_005273353.1:p.Thr5446=
XM_005273297.3:c.16338T>G	XP_005273354.1:p.Thr5446=
XM_005273298.3:c.16305T>G	XP_005273355.1:p.Thr5435=
XM_005273299.3:c.16086T>G	XP_005273356.1:p.Thr5362=
XM_005273300.3:c.16086T>G	XP_005273357.1:p.Thr5362=
XM_005273301.3:c.16086T>G	XP_005273358.1:p.Thr5362=
XM_005273302.3:c.16062T>G	XP_005273359.1:p.Thr5354=
XM_005273304.3:c.15822T>G	XP_005273361.1:p.Thr5274=
XM_005273305.3:c.15558T>G	XP_005273362.1:p.Thr5186=
XM_005273307.3:c.15492T>G	XP_005273364.1:p.Thr5164=
XM_005273309.3:c.16614T>G	XP_005273366.1:p.Thr5538=
XM_005273310.3:c.16614T>G	XP_005273367.1:p.Thr5538=
XM_006711819.2:c.16464T>G	XP_006711882.1:p.Thr5488=
XM_006711820.2:c.16350T>G	XP_006711883.1:p.Thr5450=
XM_006711821.2:c.16074T>G	XP_006711884.1:p.Thr5358=
XM_006711822.2:c.16038T>G	XP_006711885.1:p.Thr5346=
XM_006711823.2:c.16038T>G	XP_006711886.1:p.Thr5346=
XM_006711824.2:c.15030T>G	XP_006711887.1:p.Thr5010=
XM_006711825.2:c.13710T>G	XP_006711888.1:p.Thr4570=
XM_006711826.2:c.16614T>G	XP_006711889.1:p.Thr5538=
XM_006711827.2:c.14454T>G	XP_006711890.1:p.Thr4818=
XM_006711828.2:c.16314T>G	XP_006711891.1:p.Thr5438=
XM_006711829.2:c.14178T>G	XP_006711892.1:p.Thr4726=
XM_011544290.1:c.16338T>G	XP_011542592.1:p.Thr5446=
XM_011544291.1:c.16041T>G	XP_011542593.1:p.Thr5347=
XM_011544292.1:c.15822T>G	XP_011542594.1:p.Thr5274=
XM_011544293.1:c.15822T>G	XP_011542595.1:p.Thr5274=
XM_011544294.1:c.15822T>G	XP_011542596.1:p.Thr5274=
XM_011544295.1:c.15510T>G	XP_011542597.1:p.Thr5170=
XM_011544296.1:c.14766T>G	XP_011542598.1:p.Thr4922=
XM_011544297.1:c.14454T>G	XP_011542599.1:p.Thr4818=
XM_011544299.1:c.14178T>G	XP_011542601.1:p.Thr4726=
XM_005273287.5:c.16614T>G	XP_005273344.1:p.Thr5538=
XM_005273291.5:c.16578T>G	XP_005273348.1:p.Thr5526=
XM_005273298.5:c.16305T>G	XP_005273355.1:p.Thr5435=
XM_005273307.5:c.15492T>G	XP_005273364.1:p.Thr5164=
XM_006711822.4:c.16038T>G	XP_006711885.1:p.Thr5346=
XM_006711823.4:c.16038T>G	XP_006711886.1:p.Thr5346=
XM_006711827.4:c.14454T>G	XP_006711890.1:p.Thr4818=
XM_006711829.4:c.14178T>G	XP_006711892.1:p.Thr4726=
XM_011544297.3:c.14454T>G	XP_011542599.1:p.Thr4818=
XM_011544299.3:c.14178T>G	XP_011542601.1:p.Thr4726=
XM_017002443.2:c.16659T>G	XP_016857932.1:p.Thr5553=
XM_017002444.2:c.16659T>G	XP_016857933.1:p.Thr5553=
XM_017002445.2:c.16659T>G	XP_016857934.1:p.Thr5553=
XM_017002446.2:c.16659T>G	XP_016857935.1:p.Thr5553=
XM_017002447.2:c.16659T>G	XP_016857936.1:p.Thr5553=
XM_017002448.2:c.16509T>G	XP_016857937.1:p.Thr5503=
XM_017002449.2:c.16395T>G	XP_016857938.1:p.Thr5465=
XM_017002450.2:c.16395T>G	XP_016857939.1:p.Thr5465=
XM_017002451.2:c.16395T>G	XP_016857940.1:p.Thr5465=
XM_017002452.2:c.16395T>G	XP_016857941.1:p.Thr5465=
XM_017002453.2:c.16383T>G	XP_016857942.1:p.Thr5461=
XM_017002454.2:c.16383T>G	XP_016857943.1:p.Thr5461=
XM_017002455.2:c.16383T>G	XP_016857944.1:p.Thr5461=
XM_017002456.2:c.16383T>G	XP_016857945.1:p.Thr5461=
XM_017002457.2:c.16383T>G	XP_016857946.1:p.Thr5461=
XM_017002458.2:c.16131T>G	XP_016857947.1:p.Thr5377=
XM_017002459.2:c.16131T>G	XP_016857948.1:p.Thr5377=
XM_017002460.2:c.16131T>G	XP_016857949.1:p.Thr5377=
XM_017002461.2:c.16119T>G	XP_016857950.1:p.Thr5373=
XM_017002462.2:c.16107T>G	XP_016857951.1:p.Thr5369=
XM_017002463.2:c.16086T>G	XP_016857952.1:p.Thr5362=
XM_017002464.2:c.16038T>G	XP_016857953.1:p.Thr5346=
XM_017002465.2:c.15867T>G	XP_016857954.1:p.Thr5289=
XM_017002466.2:c.15867T>G	XP_016857955.1:p.Thr5289=
XM_017002467.2:c.15867T>G	XP_016857956.1:p.Thr5289=
XM_017002468.2:c.15603T>G	XP_016857957.1:p.Thr5201=
XM_017002469.2:c.15075T>G	XP_016857958.1:p.Thr5025=
XM_017002470.2:c.13755T>G	XP_016857959.1:p.Thr4585=
XM_017002471.2:c.16659T>G	XP_016857960.1:p.Thr5553=
XM_017002472.2:c.16659T>G	XP_016857961.1:p.Thr5553=
XM_017002473.2:c.16659T>G	XP_016857962.1:p.Thr5553=
XR_001737476.2:n.23542T>G
NM_052843.4:c.13443T>G	NP_443075.3:p.Thr4481=
NM_001271223.3:c.16314T>G	NP_001258152.2:p.Thr5438=
NM_001386125.1:c.16314T>G MANE Select	NP_001373054.1:p.Thr5438=