Canonical Allele Identifier: CA1619890562

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164935A= , CM000668.2:g.33164935A=	GRCh38
NC_000006.11:g.33132712A= , CM000668.1:g.33132712A=	GRCh37
NC_000006.10:g.33240690A=	NCBI36
NG_011589.1:g.32534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.586T=
ENST00000341947.7:c.4780T= MANE Select	ENSP00000339915.2:p.Cys1594=
ENST00000341947.6:c.4780T=	ENSP00000339915.2:p.Cys1594=
ENST00000361917.5:c.4459T=	ENSP00000355123.1:p.Cys1487=
ENST00000374708.8:c.4522T=	ENSP00000363840.4:p.Cys1508=
ENST00000477772.1:n.570T=
NM_080679.2:c.4459T=	NP_542410.2:p.Cys1487=
NM_080680.2:c.4780T=	NP_542411.2:p.Cys1594=
NM_080681.2:c.4522T=	NP_542412.2:p.Cys1508=
XM_011514298.1:c.3934T=	XP_011512600.1:p.Cys1312=
XM_011514299.1:c.4066T=	XP_011512601.1:p.Cys1356=
XM_011514300.1:c.3886T=	XP_011512602.1:p.Cys1296=
XM_011514301.1:c.3823T=	XP_011512603.1:p.Cys1275=
XM_011514302.1:c.3667T=	XP_011512604.1:p.Cys1223=
XM_011514299.2:c.4066T=	XP_011512601.1:p.Cys1356=
XM_011514300.2:c.3886T=	XP_011512602.1:p.Cys1296=
XM_011514302.2:c.3667T=	XP_011512604.1:p.Cys1223=
XM_017010250.1:c.4780T=	XP_016865739.1:p.Cys1594=
XM_017010251.2:c.3598T=	XP_016865740.1:p.Cys1200=
NM_080680.3:c.4780T= MANE Select	NP_542411.2:p.Cys1594=
NM_080681.3:c.4522T=	NP_542412.2:p.Cys1508=
NM_080679.3:c.4459T=	NP_542410.2:p.Cys1487=