Canonical Allele Identifier: CA1185243155

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102914737C= , CM000663.2:g.102914737C=	GRCh38
NC_000001.10:g.103380293C= , CM000663.1:g.103380293C=	GRCh37
NC_000001.9:g.103152881C=	NCBI36
NG_008033.1:g.198760G=
NG_008033.2:g.198760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3891G= MANE Select	ENSP00000359114.3:p.Gly1297=
ENST00000353414.8:c.3774G=	ENSP00000302551.6:p.Gly1258=
ENST00000358392.6:c.3927G=	ENSP00000351163.2:p.Gly1309=
ENST00000370096.7:c.3891G=	ENSP00000359114.3:p.Gly1297=
ENST00000512756.5:c.3543G=	ENSP00000426533.1:p.Gly1181=
ENST00000635193.1:c.3225G=
NM_001190709.1:c.3774G=	NP_001177638.1:p.Gly1258=
NM_001854.3:c.3891G=	NP_001845.3:p.Gly1297=
NM_080629.2:c.3927G=	NP_542196.2:p.Gly1309=
NM_080630.3:c.3543G=	NP_542197.3:p.Gly1181=
XM_011540719.1:c.3891G=	XP_011539021.1:p.Gly1297=
XM_011540720.1:c.2124G=	XP_011539022.1:p.Gly708=
XM_011540721.1:c.1479G=	XP_011539023.1:p.Gly493=
NR_134980.1:n.4225G=
XM_017000334.1:c.4044G=	XP_016855823.1:p.Gly1348=
XM_017000335.1:c.4038G=	XP_016855824.1:p.Gly1346=
XM_017000336.1:c.4044G=	XP_016855825.1:p.Gly1348=
XM_017000337.1:c.2442G=	XP_016855826.1:p.Gly814=
NM_001854.4:c.3891G= MANE Select	NP_001845.3:p.Gly1297=
NM_080630.4:c.3543G=	NP_542197.3:p.Gly1181=
NR_134980.2:n.4251G=
NM_001190709.2:c.3774G=	NP_001177638.1:p.Gly1258=
NM_080629.3:c.3927G=	NP_542196.2:p.Gly1309=