Canonical Allele Identifier: CA2034476822

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47978313A= , CM000674.2:g.47978313A=	GRCh38
NC_000012.11:g.48372096A= , CM000674.1:g.48372096A=	GRCh37
NC_000012.10:g.46658363A=	NCBI36
NG_008072.1:g.31190T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.2774T=	ENSP00000338213.6:p.Phe925=
ENST00000380518.8:c.2981T= MANE Select	ENSP00000369889.3:p.Phe994=
ENST00000337299.6:c.2774T=	ENSP00000338213.6:p.Phe925=
ENST00000380518.7:c.2981T=	ENSP00000369889.3:p.Phe994=
ENST00000493991.5:n.2067T=
NM_001844.4:c.2981T=	NP_001835.3:p.Phe994=
NM_033150.2:c.2774T=	NP_149162.2:p.Phe925=
XM_006719242.2:c.3125T=	XP_006719305.2:p.Phe1042=
XM_011537928.1:c.3125T=	XP_011536230.1:p.Phe1042=
XM_011537929.1:c.3125T=	XP_011536231.1:p.Phe1042=
XM_011537930.1:c.3125T=	XP_011536232.1:p.Phe1042=
XM_011537931.1:c.3125T=	XP_011536233.1:p.Phe1042=
XM_011537932.1:c.3125T=	XP_011536234.1:p.Phe1042=
XM_011537933.1:c.3125T=	XP_011536235.1:p.Phe1042=
XM_011537934.1:c.3122T=	XP_011536236.1:p.Phe1041=
XM_011537935.1:c.2069T=	XP_011536237.1:p.Phe690=
XM_017018828.1:c.3125T=	XP_016874317.1:p.Phe1042=
XM_017018829.1:c.3122T=	XP_016874318.1:p.Phe1041=
XM_017018830.1:c.2915T=	XP_016874319.1:p.Phe972=
XM_017018831.2:c.2435T=	XP_016874320.1:p.Phe812=
NM_001844.5:c.2981T= MANE Select	NP_001835.3:p.Phe994=
NM_033150.3:c.2774T=	NP_149162.2:p.Phe925=