Canonical Allele Identifier: CA384533535

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48367939T>G (hg19) ; chr12:g.47974156T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47974156T>G , CM000674.2:g.47974156T>G	GRCh38
NC_000012.11:g.48367939T>G , CM000674.1:g.48367939T>G	GRCh37
NC_000012.10:g.46654206T>G	NCBI36
NG_008072.1:g.35347A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.4043A>C	ENSP00000338213.6:p.Asn1348Thr
ENST00000380518.8:c.4250A>C MANE Select	ENSP00000369889.3:p.Asn1417Thr
ENST00000337299.6:c.4043A>C	ENSP00000338213.6:p.Asn1348Thr
ENST00000380518.7:c.4250A>C	ENSP00000369889.3:p.Asn1417Thr
ENST00000493991.5:n.3336A>C
NM_001844.4:c.4250A>C	NP_001835.3:p.Asn1417Thr
NM_033150.2:c.4043A>C	NP_149162.2:p.Asn1348Thr
XM_006719242.2:c.4394A>C	XP_006719305.2:p.Asn1465Thr
XM_011537928.1:c.4394A>C	XP_011536230.1:p.Asn1465Thr
XM_011537929.1:c.4394A>C	XP_011536231.1:p.Asn1465Thr
XM_011537930.1:c.4394A>C	XP_011536232.1:p.Asn1465Thr
XM_011537931.1:c.4394A>C	XP_011536233.1:p.Asn1465Thr
XM_011537932.1:c.4394A>C	XP_011536234.1:p.Asn1465Thr
XM_011537933.1:c.4394A>C	XP_011536235.1:p.Asn1465Thr
XM_011537934.1:c.4391A>C	XP_011536236.1:p.Asn1464Thr
XM_011537935.1:c.3338A>C	XP_011536237.1:p.Asn1113Thr
XM_017018828.1:c.4394A>C	XP_016874317.1:p.Asn1465Thr
XM_017018829.1:c.4391A>C	XP_016874318.1:p.Asn1464Thr
XM_017018830.1:c.4184A>C	XP_016874319.1:p.Asn1395Thr
XM_017018831.2:c.3704A>C	XP_016874320.1:p.Asn1235Thr
NM_001844.5:c.4250A>C MANE Select	NP_001835.3:p.Asn1417Thr
NM_033150.3:c.4043A>C	NP_149162.2:p.Asn1348Thr