Canonical Allele Identifier: CA339874235

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40301337C>T , CM000663.2:g.40301337C>T	GRCh38
NC_000001.10:g.40767009C>T , CM000663.1:g.40767009C>T	GRCh37
NC_000001.9:g.40539596C>T	NCBI36
NG_008031.1:g.20931G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.1915G>A MANE Select	ENSP00000361834.3:p.Asp639Asn
ENST00000372748.7:c.1915G>A	ENSP00000361834.3:p.Asp639Asn
ENST00000482722.5:n.2218G>A
NM_001852.3:c.1915G>A	NP_001843.1:p.Asp639Asn
XM_006710365.2:c.1915G>A	XP_006710428.1:p.Asp639Asn
XM_011540714.1:c.1927G>A	XP_011539016.1:p.Asp643Asn
XM_011540715.1:c.1645G>A	XP_011539017.1:p.Asp549Asn
XM_011540716.1:c.1645G>A	XP_011539018.1:p.Asp549Asn
XM_011540717.1:c.1372G>A	XP_011539019.1:p.Asp458Asn
XM_006710365.3:c.1915G>A	XP_006710428.1:p.Asp639Asn
XM_011540715.2:c.1645G>A	XP_011539017.1:p.Asp549Asn
XM_011540716.2:c.1645G>A	XP_011539018.1:p.Asp549Asn
XM_011540717.2:c.1372G>A	XP_011539019.1:p.Asp458Asn
XM_017000332.1:c.1927G>A	XP_016855821.1:p.Asp643Asn
XM_017000333.1:c.1633G>A	XP_016855822.1:p.Asp545Asn
NM_001852.4:c.1915G>A MANE Select	NP_001843.1:p.Asp639Asn