Canonical Allele Identifier: CA1619889669

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164353C= , CM000668.2:g.33164353C=	GRCh38
NC_000006.11:g.33132130C= , CM000668.1:g.33132130C=	GRCh37
NC_000006.10:g.33240108C=	NCBI36
NG_011589.1:g.33116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.790G=
ENST00000341947.7:c.4984G= MANE Select	ENSP00000339915.2:p.Gly1662=
ENST00000341947.6:c.4984G=	ENSP00000339915.2:p.Gly1662=
ENST00000361917.5:c.4663G=	ENSP00000355123.1:p.Gly1555=
ENST00000374708.8:c.4726G=	ENSP00000363840.4:p.Gly1576=
ENST00000477772.1:n.774G=
NM_080679.2:c.4663G=	NP_542410.2:p.Gly1555=
NM_080680.2:c.4984G=	NP_542411.2:p.Gly1662=
NM_080681.2:c.4726G=	NP_542412.2:p.Gly1576=
XM_011514298.1:c.4138G=	XP_011512600.1:p.Gly1380=
XM_011514299.1:c.4270G=	XP_011512601.1:p.Gly1424=
XM_011514300.1:c.4090G=	XP_011512602.1:p.Gly1364=
XM_011514301.1:c.4027G=	XP_011512603.1:p.Gly1343=
XM_011514302.1:c.3871G=	XP_011512604.1:p.Gly1291=
XM_011514299.2:c.4270G=	XP_011512601.1:p.Gly1424=
XM_011514300.2:c.4090G=	XP_011512602.1:p.Gly1364=
XM_011514302.2:c.3871G=	XP_011512604.1:p.Gly1291=
XM_017010250.1:c.4984G=	XP_016865739.1:p.Gly1662=
XM_017010251.2:c.3802G=	XP_016865740.1:p.Gly1268=
NM_080680.3:c.4984G= MANE Select	NP_542411.2:p.Gly1662=
NM_080681.3:c.4726G=	NP_542412.2:p.Gly1576=
NM_080679.3:c.4663G=	NP_542410.2:p.Gly1555=