Canonical Allele Identifier: CA1619889799

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164413G= , CM000668.2:g.33164413G=	GRCh38
NC_000006.11:g.33132190G= , CM000668.1:g.33132190G=	GRCh37
NC_000006.10:g.33240168G=	NCBI36
NG_011589.1:g.33056C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.730C=
ENST00000341947.7:c.4924C= MANE Select	ENSP00000339915.2:p.Leu1642=
ENST00000341947.6:c.4924C=	ENSP00000339915.2:p.Leu1642=
ENST00000361917.5:c.4603C=	ENSP00000355123.1:p.Leu1535=
ENST00000374708.8:c.4666C=	ENSP00000363840.4:p.Leu1556=
ENST00000477772.1:n.714C=
NM_080679.2:c.4603C=	NP_542410.2:p.Leu1535=
NM_080680.2:c.4924C=	NP_542411.2:p.Leu1642=
NM_080681.2:c.4666C=	NP_542412.2:p.Leu1556=
XM_011514298.1:c.4078C=	XP_011512600.1:p.Leu1360=
XM_011514299.1:c.4210C=	XP_011512601.1:p.Leu1404=
XM_011514300.1:c.4030C=	XP_011512602.1:p.Leu1344=
XM_011514301.1:c.3967C=	XP_011512603.1:p.Leu1323=
XM_011514302.1:c.3811C=	XP_011512604.1:p.Leu1271=
XM_011514299.2:c.4210C=	XP_011512601.1:p.Leu1404=
XM_011514300.2:c.4030C=	XP_011512602.1:p.Leu1344=
XM_011514302.2:c.3811C=	XP_011512604.1:p.Leu1271=
XM_017010250.1:c.4924C=	XP_016865739.1:p.Leu1642=
XM_017010251.2:c.3742C=	XP_016865740.1:p.Leu1248=
NM_080680.3:c.4924C= MANE Select	NP_542411.2:p.Leu1642=
NM_080681.3:c.4666C=	NP_542412.2:p.Leu1556=
NM_080679.3:c.4603C=	NP_542410.2:p.Leu1535=