Canonical Allele Identifier: CA1185272071

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979093G= , CM000663.2:g.102979093G=	GRCh38
NC_000001.10:g.103444649G= , CM000663.1:g.103444649G=	GRCh37
NC_000001.9:g.103217237G=	NCBI36
NG_008033.1:g.134404C=
NG_008033.2:g.134404C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2622C= MANE Select	ENSP00000359114.3:p.Gly874=
ENST00000353414.8:c.2505C=	ENSP00000302551.6:p.Gly835=
ENST00000358392.6:c.2658C=	ENSP00000351163.2:p.Gly886=
ENST00000370096.7:c.2622C=	ENSP00000359114.3:p.Gly874=
ENST00000512756.5:c.2274C=	ENSP00000426533.1:p.Gly758=
ENST00000635193.1:c.1956C=
NM_001190709.1:c.2505C=	NP_001177638.1:p.Gly835=
NM_001854.3:c.2622C=	NP_001845.3:p.Gly874=
NM_080629.2:c.2658C=	NP_542196.2:p.Gly886=
NM_080630.3:c.2274C=	NP_542197.3:p.Gly758=
XM_011540719.1:c.2622C=	XP_011539021.1:p.Gly874=
XM_011540720.1:c.855C=	XP_011539022.1:p.Gly285=
XM_011540721.1:c.210C=	XP_011539023.1:p.Gly70=
XR_946545.1:n.3036C=
NR_134980.1:n.2956C=
XM_017000334.1:c.2775C=	XP_016855823.1:p.Gly925=
XM_017000335.1:c.2769C=	XP_016855824.1:p.Gly923=
XM_017000336.1:c.2775C=	XP_016855825.1:p.Gly925=
XM_017000337.1:c.1173C=	XP_016855826.1:p.Gly391=
NM_001854.4:c.2622C= MANE Select	NP_001845.3:p.Gly874=
NM_080630.4:c.2274C=	NP_542197.3:p.Gly758=
NR_134980.2:n.2982C=
NM_001190709.2:c.2505C=	NP_001177638.1:p.Gly835=
NM_080629.3:c.2658C=	NP_542196.2:p.Gly886=