Canonical Allele Identifier: CA384533627

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48367982C>T (hg19) ; chr12:g.47974199C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47974199C>T , CM000674.2:g.47974199C>T	GRCh38
NC_000012.11:g.48367982C>T , CM000674.1:g.48367982C>T	GRCh37
NC_000012.10:g.46654249C>T	NCBI36
NG_008072.1:g.35304G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.4000G>A	ENSP00000338213.6:p.Ala1334Thr
ENST00000380518.8:c.4207G>A MANE Select	ENSP00000369889.3:p.Ala1403Thr
ENST00000337299.6:c.4000G>A	ENSP00000338213.6:p.Ala1334Thr
ENST00000380518.7:c.4207G>A	ENSP00000369889.3:p.Ala1403Thr
ENST00000493991.5:n.3293G>A
NM_001844.4:c.4207G>A	NP_001835.3:p.Ala1403Thr
NM_033150.2:c.4000G>A	NP_149162.2:p.Ala1334Thr
XM_006719242.2:c.4351G>A	XP_006719305.2:p.Ala1451Thr
XM_011537928.1:c.4351G>A	XP_011536230.1:p.Ala1451Thr
XM_011537929.1:c.4351G>A	XP_011536231.1:p.Ala1451Thr
XM_011537930.1:c.4351G>A	XP_011536232.1:p.Ala1451Thr
XM_011537931.1:c.4351G>A	XP_011536233.1:p.Ala1451Thr
XM_011537932.1:c.4351G>A	XP_011536234.1:p.Ala1451Thr
XM_011537933.1:c.4351G>A	XP_011536235.1:p.Ala1451Thr
XM_011537934.1:c.4348G>A	XP_011536236.1:p.Ala1450Thr
XM_011537935.1:c.3295G>A	XP_011536237.1:p.Ala1099Thr
XM_017018828.1:c.4351G>A	XP_016874317.1:p.Ala1451Thr
XM_017018829.1:c.4348G>A	XP_016874318.1:p.Ala1450Thr
XM_017018830.1:c.4141G>A	XP_016874319.1:p.Ala1381Thr
XM_017018831.2:c.3661G>A	XP_016874320.1:p.Ala1221Thr
NM_001844.5:c.4207G>A MANE Select	NP_001835.3:p.Ala1403Thr
NM_033150.3:c.4000G>A	NP_149162.2:p.Ala1334Thr