Canonical Allele Identifier: CA1619889775

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164402G= , CM000668.2:g.33164402G=	GRCh38
NC_000006.11:g.33132179G= , CM000668.1:g.33132179G=	GRCh37
NC_000006.10:g.33240157G=	NCBI36
NG_011589.1:g.33067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.741C=
ENST00000341947.7:c.4935C= MANE Select	ENSP00000339915.2:p.Val1645=
ENST00000341947.6:c.4935C=	ENSP00000339915.2:p.Val1645=
ENST00000361917.5:c.4614C=	ENSP00000355123.1:p.Val1538=
ENST00000374708.8:c.4677C=	ENSP00000363840.4:p.Val1559=
ENST00000477772.1:n.725C=
NM_080679.2:c.4614C=	NP_542410.2:p.Val1538=
NM_080680.2:c.4935C=	NP_542411.2:p.Val1645=
NM_080681.2:c.4677C=	NP_542412.2:p.Val1559=
XM_011514298.1:c.4089C=	XP_011512600.1:p.Val1363=
XM_011514299.1:c.4221C=	XP_011512601.1:p.Val1407=
XM_011514300.1:c.4041C=	XP_011512602.1:p.Val1347=
XM_011514301.1:c.3978C=	XP_011512603.1:p.Val1326=
XM_011514302.1:c.3822C=	XP_011512604.1:p.Val1274=
XM_011514299.2:c.4221C=	XP_011512601.1:p.Val1407=
XM_011514300.2:c.4041C=	XP_011512602.1:p.Val1347=
XM_011514302.2:c.3822C=	XP_011512604.1:p.Val1274=
XM_017010250.1:c.4935C=	XP_016865739.1:p.Val1645=
XM_017010251.2:c.3753C=	XP_016865740.1:p.Val1251=
NM_080680.3:c.4935C= MANE Select	NP_542411.2:p.Val1645=
NM_080681.3:c.4677C=	NP_542412.2:p.Val1559=
NM_080679.3:c.4614C=	NP_542410.2:p.Val1538=