Canonical Allele Identifier: CA1619900305

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33179077C= , CM000668.2:g.33179077C=	GRCh38
NC_000006.11:g.33146854C= , CM000668.1:g.33146854C=	GRCh37
NC_000006.10:g.33254832C=	NCBI36
NG_011589.1:g.18392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361917.6:c.234G=
ENST00000341947.7:c.1607G= MANE Select	ENSP00000339915.2:p.Arg536=
ENST00000341947.6:c.1607G=	ENSP00000339915.2:p.Arg536=
ENST00000361917.5:c.1286G=	ENSP00000355123.1:p.Arg429=
ENST00000374708.8:c.1349G=	ENSP00000363840.4:p.Arg450=
ENST00000457788.5:c.1607G=	ENSP00000405520.1:p.Arg536=
NM_080679.2:c.1286G=	NP_542410.2:p.Arg429=
NM_080680.2:c.1607G=	NP_542411.2:p.Arg536=
NM_080681.2:c.1349G=	NP_542412.2:p.Arg450=
XM_011514298.1:c.761G=	XP_011512600.1:p.Arg254=
XM_011514299.1:c.893G=	XP_011512601.1:p.Arg298=
XM_011514300.1:c.713G=	XP_011512602.1:p.Arg238=
XM_011514301.1:c.650G=	XP_011512603.1:p.Arg217=
XM_011514302.1:c.494G=	XP_011512604.1:p.Arg165=
XM_011514299.2:c.893G=	XP_011512601.1:p.Arg298=
XM_011514300.2:c.713G=	XP_011512602.1:p.Arg238=
XM_011514302.2:c.494G=	XP_011512604.1:p.Arg165=
XM_017010250.1:c.1607G=	XP_016865739.1:p.Arg536=
XM_017010251.2:c.425G=	XP_016865740.1:p.Arg142=
NM_080680.3:c.1607G= MANE Select	NP_542411.2:p.Arg536=
NM_080681.3:c.1349G=	NP_542412.2:p.Arg450=
NM_080679.3:c.1286G=	NP_542410.2:p.Arg429=