Canonical Allele Identifier: CA384555632

Gene: COL2A1

Linked Data

• gnomAD v4: 12-47992898-T-A
• MyVariant Identifiers: chr12:g.48386681T>A (hg19) ; chr12:g.47992898T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47992898T>A , CM000674.2:g.47992898T>A	GRCh38
NC_000012.11:g.48386681T>A , CM000674.1:g.48386681T>A	GRCh37
NC_000012.10:g.46672948T>A	NCBI36
NG_008072.1:g.16605A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.796A>T	ENSP00000338213.6:p.Thr266Ser
ENST00000380518.8:c.1003A>T MANE Select	ENSP00000369889.3:p.Thr335Ser
ENST00000337299.6:c.796A>T	ENSP00000338213.6:p.Thr266Ser
ENST00000380518.7:c.1003A>T	ENSP00000369889.3:p.Thr335Ser
NM_001844.4:c.1003A>T	NP_001835.3:p.Thr335Ser
NM_033150.2:c.796A>T	NP_149162.2:p.Thr266Ser
XM_006719242.2:c.1147A>T	XP_006719305.2:p.Thr383Ser
XM_011537928.1:c.1147A>T	XP_011536230.1:p.Thr383Ser
XM_011537929.1:c.1147A>T	XP_011536231.1:p.Thr383Ser
XM_011537930.1:c.1147A>T	XP_011536232.1:p.Thr383Ser
XM_011537931.1:c.1147A>T	XP_011536233.1:p.Thr383Ser
XM_011537932.1:c.1147A>T	XP_011536234.1:p.Thr383Ser
XM_011537933.1:c.1147A>T	XP_011536235.1:p.Thr383Ser
XM_011537934.1:c.1144A>T	XP_011536236.1:p.Thr382Ser
XM_017018828.1:c.1147A>T	XP_016874317.1:p.Thr383Ser
XM_017018829.1:c.1144A>T	XP_016874318.1:p.Thr382Ser
XM_017018830.1:c.937A>T	XP_016874319.1:p.Thr313Ser
XM_017018831.2:c.457A>T	XP_016874320.1:p.Thr153Ser
NM_001844.5:c.1003A>T MANE Select	NP_001835.3:p.Thr335Ser
NM_033150.3:c.796A>T	NP_149162.2:p.Thr266Ser