Canonical Allele Identifier: CA1164340611

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40314352C= , CM000663.2:g.40314352C=	GRCh38
NC_000001.10:g.40780024C= , CM000663.1:g.40780024C=	GRCh37
NC_000001.9:g.40552611C=	NCBI36
NG_008031.1:g.7916G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.186G= MANE Select	ENSP00000361834.3:p.Pro62=
ENST00000417105.6:c.-97G=	ENSP00000388493.2:n.-97G=
ENST00000461118.6:n.752G=
ENST00000488463.6:n.237G=
ENST00000642679.1:c.-97G=	ENSP00000495407.1:n.-97G=
ENST00000372736.3:c.150+1238G=	ENSP00000361821.3:n.150+1238G=
ENST00000372748.7:c.186G=	ENSP00000361834.3:p.Pro62=
ENST00000417105.5:c.151G=
ENST00000461118.5:n.755G=
ENST00000482722.5:n.146G=
ENST00000488463.5:n.237G=
ENST00000496215.5:n.335G=
NM_001852.3:c.186G=	NP_001843.1:p.Pro62=
XM_006710365.2:c.186G=	XP_006710428.1:p.Pro62=
XM_011540714.1:c.186G=	XP_011539016.1:p.Pro62=
XM_011540715.1:c.-97G=	XP_011539017.1:n.-97G=
XM_011540716.1:c.-97G=	XP_011539018.1:n.-97G=
XM_011540717.1:c.-701G=	XP_011539019.1:n.-701G=
XM_011540718.1:c.186G=	XP_011539020.1:p.Pro62=
XM_006710365.3:c.186G=	XP_006710428.1:p.Pro62=
XM_011540715.2:c.-97G=	XP_011539017.1:n.-97G=
XM_011540716.2:c.-97G=	XP_011539018.1:n.-97G=
XM_011540717.2:c.-701G=	XP_011539019.1:n.-701G=
XM_017000332.1:c.186G=	XP_016855821.1:p.Pro62=
XM_017000333.1:c.-97G=	XP_016855822.1:n.-97G=
NM_001852.4:c.186G= MANE Select	NP_001843.1:p.Pro62=