Canonical Allele Identifier: CA1619899522

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33177216C= , CM000668.2:g.33177216C=	GRCh38
NC_000006.11:g.33144993C= , CM000668.1:g.33144993C=	GRCh37
NC_000006.10:g.33252971C=	NCBI36
NG_011589.1:g.20253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361917.6:c.554G=
ENST00000341947.7:c.1981G= MANE Select	ENSP00000339915.2:p.Gly661=
ENST00000341947.6:c.1981G=	ENSP00000339915.2:p.Gly661=
ENST00000361917.5:c.1660G=	ENSP00000355123.1:p.Gly554=
ENST00000374708.8:c.1723G=	ENSP00000363840.4:p.Gly575=
ENST00000477772.1:n.200G=
NM_080679.2:c.1660G=	NP_542410.2:p.Gly554=
NM_080680.2:c.1981G=	NP_542411.2:p.Gly661=
NM_080681.2:c.1723G=	NP_542412.2:p.Gly575=
XM_011514298.1:c.1135G=	XP_011512600.1:p.Gly379=
XM_011514299.1:c.1267G=	XP_011512601.1:p.Gly423=
XM_011514300.1:c.1087G=	XP_011512602.1:p.Gly363=
XM_011514301.1:c.1024G=	XP_011512603.1:p.Gly342=
XM_011514302.1:c.868G=	XP_011512604.1:p.Gly290=
XM_011514299.2:c.1267G=	XP_011512601.1:p.Gly423=
XM_011514300.2:c.1087G=	XP_011512602.1:p.Gly363=
XM_011514302.2:c.868G=	XP_011512604.1:p.Gly290=
XM_017010250.1:c.1981G=	XP_016865739.1:p.Gly661=
XM_017010251.2:c.799G=	XP_016865740.1:p.Gly267=
NM_080680.3:c.1981G= MANE Select	NP_542411.2:p.Gly661=
NM_080681.3:c.1723G=	NP_542412.2:p.Gly575=
NM_080679.3:c.1660G=	NP_542410.2:p.Gly554=