Canonical Allele Identifier: CA1139921521

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40307477T= , CM000663.2:g.40307477T=	GRCh38
NC_000001.10:g.40773149T= , CM000663.1:g.40773149T=	GRCh37
NC_000001.9:g.40545736T=	NCBI36
NG_008031.1:g.14791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.977A= MANE Select	ENSP00000361834.3:p.Gln326=
ENST00000372748.7:c.977A=	ENSP00000361834.3:p.Gln326=
ENST00000482722.5:n.1280A=
NM_001852.3:c.977A=	NP_001843.1:p.Gln326=
XM_006710365.2:c.977A=	XP_006710428.1:p.Gln326=
XM_011540714.1:c.989A=	XP_011539016.1:p.Gln330=
XM_011540715.1:c.707A=	XP_011539017.1:p.Gln236=
XM_011540716.1:c.707A=	XP_011539018.1:p.Gln236=
XM_011540717.1:c.434A=	XP_011539019.1:p.Gln145=
XM_011540718.1:c.989A=	XP_011539020.1:p.Gln330=
XM_006710365.3:c.977A=	XP_006710428.1:p.Gln326=
XM_011540715.2:c.707A=	XP_011539017.1:p.Gln236=
XM_011540716.2:c.707A=	XP_011539018.1:p.Gln236=
XM_011540717.2:c.434A=	XP_011539019.1:p.Gln145=
XM_017000332.1:c.989A=	XP_016855821.1:p.Gln330=
XM_017000333.1:c.695A=	XP_016855822.1:p.Gln232=
NM_001852.4:c.977A= MANE Select	NP_001843.1:p.Gln326=