Canonical Allele Identifier: CA1139921520

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40307451G= , CM000663.2:g.40307451G=	GRCh38
NC_000001.10:g.40773123G= , CM000663.1:g.40773123G=	GRCh37
NC_000001.9:g.40545710G=	NCBI36
NG_008031.1:g.14817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.1003C= MANE Select	ENSP00000361834.3:p.Leu335=
ENST00000372748.7:c.1003C=	ENSP00000361834.3:p.Leu335=
ENST00000482722.5:n.1306C=
NM_001852.3:c.1003C=	NP_001843.1:p.Leu335=
XM_006710365.2:c.1003C=	XP_006710428.1:p.Leu335=
XM_011540714.1:c.1015C=	XP_011539016.1:p.Leu339=
XM_011540715.1:c.733C=	XP_011539017.1:p.Leu245=
XM_011540716.1:c.733C=	XP_011539018.1:p.Leu245=
XM_011540717.1:c.460C=	XP_011539019.1:p.Leu154=
XM_011540718.1:c.1015C=	XP_011539020.1:p.Leu339=
XM_006710365.3:c.1003C=	XP_006710428.1:p.Leu335=
XM_011540715.2:c.733C=	XP_011539017.1:p.Leu245=
XM_011540716.2:c.733C=	XP_011539018.1:p.Leu245=
XM_011540717.2:c.460C=	XP_011539019.1:p.Leu154=
XM_017000332.1:c.1015C=	XP_016855821.1:p.Leu339=
XM_017000333.1:c.721C=	XP_016855822.1:p.Leu241=
NM_001852.4:c.1003C= MANE Select	NP_001843.1:p.Leu335=