Canonical Allele Identifier: CA1619889882

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164459G= , CM000668.2:g.33164459G=	GRCh38
NC_000006.11:g.33132236G= , CM000668.1:g.33132236G=	GRCh37
NC_000006.10:g.33240214G=	NCBI36
NG_011589.1:g.33010C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.684C=
ENST00000341947.7:c.4878C= MANE Select	ENSP00000339915.2:p.Asp1626=
ENST00000341947.6:c.4878C=	ENSP00000339915.2:p.Asp1626=
ENST00000361917.5:c.4557C=	ENSP00000355123.1:p.Asp1519=
ENST00000374708.8:c.4620C=	ENSP00000363840.4:p.Asp1540=
ENST00000477772.1:n.668C=
NM_080679.2:c.4557C=	NP_542410.2:p.Asp1519=
NM_080680.2:c.4878C=	NP_542411.2:p.Asp1626=
NM_080681.2:c.4620C=	NP_542412.2:p.Asp1540=
XM_011514298.1:c.4032C=	XP_011512600.1:p.Asp1344=
XM_011514299.1:c.4164C=	XP_011512601.1:p.Asp1388=
XM_011514300.1:c.3984C=	XP_011512602.1:p.Asp1328=
XM_011514301.1:c.3921C=	XP_011512603.1:p.Asp1307=
XM_011514302.1:c.3765C=	XP_011512604.1:p.Asp1255=
XM_011514299.2:c.4164C=	XP_011512601.1:p.Asp1388=
XM_011514300.2:c.3984C=	XP_011512602.1:p.Asp1328=
XM_011514302.2:c.3765C=	XP_011512604.1:p.Asp1255=
XM_017010250.1:c.4878C=	XP_016865739.1:p.Asp1626=
XM_017010251.2:c.3696C=	XP_016865740.1:p.Asp1232=
NM_080680.3:c.4878C= MANE Select	NP_542411.2:p.Asp1626=
NM_080681.3:c.4620C=	NP_542412.2:p.Asp1540=
NM_080679.3:c.4557C=	NP_542410.2:p.Asp1519=