Canonical Allele Identifier: CA1619890425

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164861G= , CM000668.2:g.33164861G=	GRCh38
NC_000006.11:g.33132638G= , CM000668.1:g.33132638G=	GRCh37
NC_000006.10:g.33240616G=	NCBI36
NG_011589.1:g.32608C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.660C=
ENST00000341947.7:c.4854C= MANE Select	ENSP00000339915.2:p.Asp1618=
ENST00000341947.6:c.4854C=	ENSP00000339915.2:p.Asp1618=
ENST00000361917.5:c.4533C=	ENSP00000355123.1:p.Asp1511=
ENST00000374708.8:c.4596C=	ENSP00000363840.4:p.Asp1532=
ENST00000477772.1:n.644C=
NM_080679.2:c.4533C=	NP_542410.2:p.Asp1511=
NM_080680.2:c.4854C=	NP_542411.2:p.Asp1618=
NM_080681.2:c.4596C=	NP_542412.2:p.Asp1532=
XM_011514298.1:c.4008C=	XP_011512600.1:p.Asp1336=
XM_011514299.1:c.4140C=	XP_011512601.1:p.Asp1380=
XM_011514300.1:c.3960C=	XP_011512602.1:p.Asp1320=
XM_011514301.1:c.3897C=	XP_011512603.1:p.Asp1299=
XM_011514302.1:c.3741C=	XP_011512604.1:p.Asp1247=
XM_011514299.2:c.4140C=	XP_011512601.1:p.Asp1380=
XM_011514300.2:c.3960C=	XP_011512602.1:p.Asp1320=
XM_011514302.2:c.3741C=	XP_011512604.1:p.Asp1247=
XM_017010250.1:c.4854C=	XP_016865739.1:p.Asp1618=
XM_017010251.2:c.3672C=	XP_016865740.1:p.Asp1224=
NM_080680.3:c.4854C= MANE Select	NP_542411.2:p.Asp1618=
NM_080681.3:c.4596C=	NP_542412.2:p.Asp1532=
NM_080679.3:c.4533C=	NP_542410.2:p.Asp1511=