Canonical Allele Identifier: CA791303

Gene: COL9A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40301816G>A , CM000663.2:g.40301816G>A	GRCh38
NC_000001.10:g.40767488G>A , CM000663.1:g.40767488G>A	GRCh37
NC_000001.9:g.40540075G>A	NCBI36
NG_008031.1:g.20452C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.1866C>T MANE Select	ENSP00000361834.3:p.Ile622=
ENST00000372748.7:c.1866C>T	ENSP00000361834.3:p.Ile622=
ENST00000466267.1:n.831C>T
ENST00000482722.5:n.2169C>T
NM_001852.3:c.1866C>T	NP_001843.1:p.Ile622=
XM_006710365.2:c.1866C>T	XP_006710428.1:p.Ile622=
XM_011540714.1:c.1878C>T	XP_011539016.1:p.Ile626=
XM_011540715.1:c.1596C>T	XP_011539017.1:p.Ile532=
XM_011540716.1:c.1596C>T	XP_011539018.1:p.Ile532=
XM_011540717.1:c.1323C>T	XP_011539019.1:p.Ile441=
XM_006710365.3:c.1866C>T	XP_006710428.1:p.Ile622=
XM_011540715.2:c.1596C>T	XP_011539017.1:p.Ile532=
XM_011540716.2:c.1596C>T	XP_011539018.1:p.Ile532=
XM_011540717.2:c.1323C>T	XP_011539019.1:p.Ile441=
XM_017000332.1:c.1878C>T	XP_016855821.1:p.Ile626=
XM_017000333.1:c.1584C>T	XP_016855822.1:p.Ile528=
NM_001852.4:c.1866C>T MANE Select	NP_001843.1:p.Ile622=