Canonical Allele Identifier: CA1619890473

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164885C= , CM000668.2:g.33164885C=	GRCh38
NC_000006.11:g.33132662C= , CM000668.1:g.33132662C=	GRCh37
NC_000006.10:g.33240640C=	NCBI36
NG_011589.1:g.32584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.636G=
ENST00000341947.7:c.4830G= MANE Select	ENSP00000339915.2:p.Glu1610=
ENST00000341947.6:c.4830G=	ENSP00000339915.2:p.Glu1610=
ENST00000361917.5:c.4509G=	ENSP00000355123.1:p.Glu1503=
ENST00000374708.8:c.4572G=	ENSP00000363840.4:p.Glu1524=
ENST00000477772.1:n.620G=
NM_080679.2:c.4509G=	NP_542410.2:p.Glu1503=
NM_080680.2:c.4830G=	NP_542411.2:p.Glu1610=
NM_080681.2:c.4572G=	NP_542412.2:p.Glu1524=
XM_011514298.1:c.3984G=	XP_011512600.1:p.Glu1328=
XM_011514299.1:c.4116G=	XP_011512601.1:p.Glu1372=
XM_011514300.1:c.3936G=	XP_011512602.1:p.Glu1312=
XM_011514301.1:c.3873G=	XP_011512603.1:p.Glu1291=
XM_011514302.1:c.3717G=	XP_011512604.1:p.Glu1239=
XM_011514299.2:c.4116G=	XP_011512601.1:p.Glu1372=
XM_011514300.2:c.3936G=	XP_011512602.1:p.Glu1312=
XM_011514302.2:c.3717G=	XP_011512604.1:p.Glu1239=
XM_017010250.1:c.4830G=	XP_016865739.1:p.Glu1610=
XM_017010251.2:c.3648G=	XP_016865740.1:p.Glu1216=
NM_080680.3:c.4830G= MANE Select	NP_542411.2:p.Glu1610=
NM_080681.3:c.4572G=	NP_542412.2:p.Glu1524=
NM_080679.3:c.4509G=	NP_542410.2:p.Glu1503=