Canonical Allele Identifier: CA10877327

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40304238C>T , CM000663.2:g.40304238C>T	GRCh38
NC_000001.10:g.40769910C>T , CM000663.1:g.40769910C>T	GRCh37
NC_000001.9:g.40542497C>T	NCBI36
NG_008031.1:g.18030G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001852.4:c.1287+82G>A MANE Select	NP_001843.1:n.1287+82G>A
ENST00000372748.8:c.1287+82G>A MANE Select	ENSP00000361834.3:n.1287+82G>A
NM_001852.3:c.1287+82G>A	NP_001843.1:n.1287+82G>A
ENST00000372748.7:c.1287+82G>A	ENSP00000361834.3:n.1287+82G>A
ENST00000427563.1:c.98+82G>A	ENSP00000407377.1:n.98+82G>A
ENST00000466267.1:n.252+82G>A
ENST00000482722.5:n.1590+82G>A
XM_006710365.2:c.1287+82G>A	XP_006710428.1:n.1287+82G>A
XM_006710365.3:c.1287+82G>A	XP_006710428.1:n.1287+82G>A
XM_011540714.1:c.1299+82G>A	XP_011539016.1:n.1299+82G>A
XM_011540715.1:c.1017+82G>A	XP_011539017.1:n.1017+82G>A
XM_011540715.2:c.1017+82G>A	XP_011539017.1:n.1017+82G>A
XM_011540716.1:c.1017+82G>A	XP_011539018.1:n.1017+82G>A
XM_011540716.2:c.1017+82G>A	XP_011539018.1:n.1017+82G>A
XM_011540717.1:c.744+82G>A	XP_011539019.1:n.744+82G>A
XM_011540717.2:c.744+82G>A	XP_011539019.1:n.744+82G>A
XM_017000332.1:c.1299+82G>A	XP_016855821.1:n.1299+82G>A
XM_017000333.1:c.1005+82G>A	XP_016855822.1:n.1005+82G>A