Canonical Allele Identifier: CA1619897561

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33172564C= , CM000668.2:g.33172564C=	GRCh38
NC_000006.11:g.33140341C= , CM000668.1:g.33140341C=	GRCh37
NC_000006.10:g.33248319C=	NCBI36
NG_011589.1:g.24905G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.2864G= MANE Select	ENSP00000339915.2:p.Gly955=
ENST00000341947.6:c.2864G=	ENSP00000339915.2:p.Gly955=
ENST00000361917.5:c.2543G=	ENSP00000355123.1:p.Gly848=
ENST00000374708.8:c.2606G=	ENSP00000363840.4:p.Gly869=
ENST00000477772.1:n.272+4445G=
NM_080679.2:c.2543G=	NP_542410.2:p.Gly848=
NM_080680.2:c.2864G=	NP_542411.2:p.Gly955=
NM_080681.2:c.2606G=	NP_542412.2:p.Gly869=
XM_011514298.1:c.2018G=	XP_011512600.1:p.Gly673=
XM_011514299.1:c.2150G=	XP_011512601.1:p.Gly717=
XM_011514300.1:c.1970G=	XP_011512602.1:p.Gly657=
XM_011514301.1:c.1907G=	XP_011512603.1:p.Gly636=
XM_011514302.1:c.1751G=	XP_011512604.1:p.Gly584=
XM_011514299.2:c.2150G=	XP_011512601.1:p.Gly717=
XM_011514300.2:c.1970G=	XP_011512602.1:p.Gly657=
XM_011514302.2:c.1751G=	XP_011512604.1:p.Gly584=
XM_017010250.1:c.2864G=	XP_016865739.1:p.Gly955=
XM_017010251.2:c.1682G=	XP_016865740.1:p.Gly561=
NM_080680.3:c.2864G= MANE Select	NP_542411.2:p.Gly955=
NM_080681.3:c.2606G=	NP_542412.2:p.Gly869=
NM_080679.3:c.2543G=	NP_542410.2:p.Gly848=