Canonical Allele Identifier: CA338120952

Gene: CAMTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7670945A>G , CM000663.2:g.7670945A>G	GRCh38
NC_000001.10:g.7731005A>G , CM000663.1:g.7731005A>G	GRCh37
NC_000001.9:g.7653592A>G	NCBI36
NG_053148.1:g.890622A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015215.4:c.2687A>G MANE Select	NP_056030.1:p.Gln896Arg
ENST00000303635.12:c.2687A>G MANE Select	ENSP00000306522.6:p.Gln896Arg
NM_001349608.1:c.2597A>G	NP_001336537.1:p.Gln866Arg
NM_001349608.2:c.2597A>G	NP_001336537.1:p.Gln866Arg
NM_001349609.1:c.2687A>G	NP_001336538.1:p.Gln896Arg
NM_001349609.2:c.2687A>G	NP_001336538.1:p.Gln896Arg
NM_001349610.1:c.2687A>G	NP_001336539.1:p.Gln896Arg
NM_001349610.2:c.2687A>G	NP_001336539.1:p.Gln896Arg
NM_001349612.1:c.2597A>G	NP_001336541.1:p.Gln866Arg
NM_001349612.2:c.2597A>G	NP_001336541.1:p.Gln866Arg
NM_001349614.1:c.-242A>G	NP_001336543.1:n.-242A>G
NM_001349617.1:c.-242A>G	NP_001336546.1:n.-242A>G
NM_001349620.1:c.-242A>G	NP_001336549.1:n.-242A>G
NM_001349621.1:c.-242A>G	NP_001336550.1:n.-242A>G
NM_001349623.1:c.-242A>G	NP_001336552.1:n.-242A>G
NM_001349625.1:c.-242A>G	NP_001336554.1:n.-242A>G
NM_001349625.2:c.-242A>G	NP_001336554.1:n.-242A>G
NM_015215.3:c.2687A>G	NP_056030.1:p.Gln896Arg
ENST00000303635.11:c.2687A>G	ENSP00000306522.6:p.Gln896Arg
ENST00000476864.2:c.2687A>G	ENSP00000452319.2:p.Gln896Arg
ENST00000700414.1:c.*2538A>G	ENSP00000514978.1:n.*2538A>G
ENST00000700415.1:c.2597A>G	ENSP00000514979.1:p.Gln866Arg
ENST00000700417.1:c.2615A>G	ENSP00000514981.1:p.Gln872Arg
ENST00000700419.1:c.950A>G	ENSP00000514983.1:p.Gln317Arg
ENST00000700420.1:c.-242A>G	ENSP00000514994.1:n.-242A>G
ENST00000700421.1:c.-242A>G	ENSP00000514995.1:n.-242A>G
ENST00000700445.1:c.414A>G
XM_011541083.1:c.2687A>G	XP_011539385.1:p.Gln896Arg
XM_011541083.2:c.2687A>G	XP_011539385.1:p.Gln896Arg
XM_011541084.1:c.2687A>G	XP_011539386.1:p.Gln896Arg
XM_011541084.2:c.2687A>G	XP_011539386.1:p.Gln896Arg
XM_011541085.1:c.2675A>G	XP_011539387.1:p.Gln892Arg
XM_011541086.1:c.2687A>G	XP_011539388.1:p.Gln896Arg
XM_011541086.3:c.2687A>G	XP_011539388.1:p.Gln896Arg
XM_011541087.1:c.2615A>G	XP_011539389.1:p.Gln872Arg
XM_011541087.2:c.2615A>G	XP_011539389.1:p.Gln872Arg
XM_011541088.1:c.2597A>G	XP_011539390.1:p.Gln866Arg
XM_011541088.2:c.2597A>G	XP_011539390.1:p.Gln866Arg
XM_011541089.1:c.2687A>G	XP_011539391.1:p.Gln896Arg
XM_011541090.1:c.2687A>G	XP_011539392.1:p.Gln896Arg
XM_011541090.3:c.2687A>G	XP_011539392.1:p.Gln896Arg
XM_011541091.1:c.2687A>G	XP_011539393.1:p.Gln896Arg
XM_011541091.2:c.2687A>G	XP_011539393.1:p.Gln896Arg
XM_011541092.1:c.2687A>G	XP_011539394.1:p.Gln896Arg
XM_011541092.3:c.2687A>G	XP_011539394.1:p.Gln896Arg
XM_017000774.2:c.2687A>G	XP_016856263.1:p.Gln896Arg
XM_017000777.1:c.2687A>G	XP_016856266.1:p.Gln896Arg
XM_017000778.1:c.2687A>G	XP_016856267.1:p.Gln896Arg
XM_024454334.1:c.-242A>G	XP_024310102.1:n.-242A>G