Canonical Allele Identifier: CA1619889833

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164431G= , CM000668.2:g.33164431G=	GRCh38
NC_000006.11:g.33132208G= , CM000668.1:g.33132208G=	GRCh37
NC_000006.10:g.33240186G=	NCBI36
NG_011589.1:g.33038C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.712C=
ENST00000341947.7:c.4906C= MANE Select	ENSP00000339915.2:p.Gln1636=
ENST00000341947.6:c.4906C=	ENSP00000339915.2:p.Gln1636=
ENST00000361917.5:c.4585C=	ENSP00000355123.1:p.Gln1529=
ENST00000374708.8:c.4648C=	ENSP00000363840.4:p.Gln1550=
ENST00000477772.1:n.696C=
NM_080679.2:c.4585C=	NP_542410.2:p.Gln1529=
NM_080680.2:c.4906C=	NP_542411.2:p.Gln1636=
NM_080681.2:c.4648C=	NP_542412.2:p.Gln1550=
XM_011514298.1:c.4060C=	XP_011512600.1:p.Gln1354=
XM_011514299.1:c.4192C=	XP_011512601.1:p.Gln1398=
XM_011514300.1:c.4012C=	XP_011512602.1:p.Gln1338=
XM_011514301.1:c.3949C=	XP_011512603.1:p.Gln1317=
XM_011514302.1:c.3793C=	XP_011512604.1:p.Gln1265=
XM_011514299.2:c.4192C=	XP_011512601.1:p.Gln1398=
XM_011514300.2:c.4012C=	XP_011512602.1:p.Gln1338=
XM_011514302.2:c.3793C=	XP_011512604.1:p.Gln1265=
XM_017010250.1:c.4906C=	XP_016865739.1:p.Gln1636=
XM_017010251.2:c.3724C=	XP_016865740.1:p.Gln1242=
NM_080680.3:c.4906C= MANE Select	NP_542411.2:p.Gln1636=
NM_080681.3:c.4648C=	NP_542412.2:p.Gln1550=
NM_080679.3:c.4585C=	NP_542410.2:p.Gln1529=