Canonical Allele Identifier: CA1619890574

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164939C= , CM000668.2:g.33164939C=	GRCh38
NC_000006.11:g.33132716C= , CM000668.1:g.33132716C=	GRCh37
NC_000006.10:g.33240694C=	NCBI36
NG_011589.1:g.32530G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.582G=
ENST00000341947.7:c.4776G= MANE Select	ENSP00000339915.2:p.Gln1592=
ENST00000341947.6:c.4776G=	ENSP00000339915.2:p.Gln1592=
ENST00000361917.5:c.4455G=	ENSP00000355123.1:p.Gln1485=
ENST00000374708.8:c.4518G=	ENSP00000363840.4:p.Gln1506=
ENST00000477772.1:n.566G=
NM_080679.2:c.4455G=	NP_542410.2:p.Gln1485=
NM_080680.2:c.4776G=	NP_542411.2:p.Gln1592=
NM_080681.2:c.4518G=	NP_542412.2:p.Gln1506=
XM_011514298.1:c.3930G=	XP_011512600.1:p.Gln1310=
XM_011514299.1:c.4062G=	XP_011512601.1:p.Gln1354=
XM_011514300.1:c.3882G=	XP_011512602.1:p.Gln1294=
XM_011514301.1:c.3819G=	XP_011512603.1:p.Gln1273=
XM_011514302.1:c.3663G=	XP_011512604.1:p.Gln1221=
XM_011514299.2:c.4062G=	XP_011512601.1:p.Gln1354=
XM_011514300.2:c.3882G=	XP_011512602.1:p.Gln1294=
XM_011514302.2:c.3663G=	XP_011512604.1:p.Gln1221=
XM_017010250.1:c.4776G=	XP_016865739.1:p.Gln1592=
XM_017010251.2:c.3594G=	XP_016865740.1:p.Gln1198=
NM_080680.3:c.4776G= MANE Select	NP_542411.2:p.Gln1592=
NM_080681.3:c.4518G=	NP_542412.2:p.Gln1506=
NM_080679.3:c.4455G=	NP_542410.2:p.Gln1485=