Canonical Allele Identifier: CA791930

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40311675G>A , CM000663.2:g.40311675G>A	GRCh38
NC_000001.10:g.40777347G>A , CM000663.1:g.40777347G>A	GRCh37
NC_000001.9:g.40549934G>A	NCBI36
NG_008031.1:g.10593C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001852.4:c.458C>T MANE Select	NP_001843.1:p.Pro153Leu
ENST00000372748.8:c.458C>T MANE Select	ENSP00000361834.3:p.Pro153Leu
NM_001852.3:c.458C>T	NP_001843.1:p.Pro153Leu
ENST00000372736.3:c.245C>T	ENSP00000361821.3:p.Pro82Leu
ENST00000372748.7:c.458C>T	ENSP00000361834.3:p.Pro153Leu
ENST00000417105.5:c.423C>T
ENST00000417105.6:c.176C>T	ENSP00000388493.2:p.Pro59Leu
ENST00000482722.5:n.761C>T
ENST00000488463.5:n.509C>T
ENST00000488463.6:n.509C>T
ENST00000496215.5:n.607C>T
XM_006710365.2:c.458C>T	XP_006710428.1:p.Pro153Leu
XM_006710365.3:c.458C>T	XP_006710428.1:p.Pro153Leu
XM_011540714.1:c.458C>T	XP_011539016.1:p.Pro153Leu
XM_011540715.1:c.176C>T	XP_011539017.1:p.Pro59Leu
XM_011540715.2:c.176C>T	XP_011539017.1:p.Pro59Leu
XM_011540716.1:c.176C>T	XP_011539018.1:p.Pro59Leu
XM_011540716.2:c.176C>T	XP_011539018.1:p.Pro59Leu
XM_011540717.1:c.-86C>T	XP_011539019.1:n.-86C>T
XM_011540717.2:c.-86C>T	XP_011539019.1:n.-86C>T
XM_011540718.1:c.458C>T	XP_011539020.1:p.Pro153Leu
XM_017000332.1:c.458C>T	XP_016855821.1:p.Pro153Leu
XM_017000333.1:c.176C>T	XP_016855822.1:p.Pro59Leu