Canonical Allele Identifier: CA1619890492

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164892C= , CM000668.2:g.33164892C=	GRCh38
NC_000006.11:g.33132669C= , CM000668.1:g.33132669C=	GRCh37
NC_000006.10:g.33240647C=	NCBI36
NG_011589.1:g.32577G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.629G=
ENST00000341947.7:c.4823G= MANE Select	ENSP00000339915.2:p.Gly1608=
ENST00000341947.6:c.4823G=	ENSP00000339915.2:p.Gly1608=
ENST00000361917.5:c.4502G=	ENSP00000355123.1:p.Gly1501=
ENST00000374708.8:c.4565G=	ENSP00000363840.4:p.Gly1522=
ENST00000477772.1:n.613G=
NM_080679.2:c.4502G=	NP_542410.2:p.Gly1501=
NM_080680.2:c.4823G=	NP_542411.2:p.Gly1608=
NM_080681.2:c.4565G=	NP_542412.2:p.Gly1522=
XM_011514298.1:c.3977G=	XP_011512600.1:p.Gly1326=
XM_011514299.1:c.4109G=	XP_011512601.1:p.Gly1370=
XM_011514300.1:c.3929G=	XP_011512602.1:p.Gly1310=
XM_011514301.1:c.3866G=	XP_011512603.1:p.Gly1289=
XM_011514302.1:c.3710G=	XP_011512604.1:p.Gly1237=
XM_011514299.2:c.4109G=	XP_011512601.1:p.Gly1370=
XM_011514300.2:c.3929G=	XP_011512602.1:p.Gly1310=
XM_011514302.2:c.3710G=	XP_011512604.1:p.Gly1237=
XM_017010250.1:c.4823G=	XP_016865739.1:p.Gly1608=
XM_017010251.2:c.3641G=	XP_016865740.1:p.Gly1214=
NM_080680.3:c.4823G= MANE Select	NP_542411.2:p.Gly1608=
NM_080681.3:c.4565G=	NP_542412.2:p.Gly1522=
NM_080679.3:c.4502G=	NP_542410.2:p.Gly1501=