Canonical Allele Identifier: CA1164336228

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40303812C= , CM000663.2:g.40303812C=	GRCh38
NC_000001.10:g.40769484C= , CM000663.1:g.40769484C=	GRCh37
NC_000001.9:g.40542071C=	NCBI36
NG_008031.1:g.18456G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372748.8:c.1396G= MANE Select	ENSP00000361834.3:p.Gly466=
ENST00000372748.7:c.1396G=	ENSP00000361834.3:p.Gly466=
ENST00000427563.1:c.207G=	ENSP00000407377.1:p.Arg69=
ENST00000466267.1:n.361G=
ENST00000482722.5:n.1699G=
NM_001852.3:c.1396G=	NP_001843.1:p.Gly466=
XM_006710365.2:c.1396G=	XP_006710428.1:p.Gly466=
XM_011540714.1:c.1408G=	XP_011539016.1:p.Gly470=
XM_011540715.1:c.1126G=	XP_011539017.1:p.Gly376=
XM_011540716.1:c.1126G=	XP_011539018.1:p.Gly376=
XM_011540717.1:c.853G=	XP_011539019.1:p.Gly285=
XM_006710365.3:c.1396G=	XP_006710428.1:p.Gly466=
XM_011540715.2:c.1126G=	XP_011539017.1:p.Gly376=
XM_011540716.2:c.1126G=	XP_011539018.1:p.Gly376=
XM_011540717.2:c.853G=	XP_011539019.1:p.Gly285=
XM_017000332.1:c.1408G=	XP_016855821.1:p.Gly470=
XM_017000333.1:c.1114G=	XP_016855822.1:p.Gly372=
NM_001852.4:c.1396G= MANE Select	NP_001843.1:p.Gly466=