Canonical Allele Identifier: CA1185260625

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102961897C= , CM000663.2:g.102961897C=	GRCh38
NC_000001.10:g.103427453C= , CM000663.1:g.103427453C=	GRCh37
NC_000001.9:g.103200041C=	NCBI36
NG_008033.1:g.151600G=
NG_008033.2:g.151600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3137G= MANE Select	ENSP00000359114.3:p.Gly1046=
ENST00000353414.8:c.3020G=	ENSP00000302551.6:p.Gly1007=
ENST00000358392.6:c.3173G=	ENSP00000351163.2:p.Gly1058=
ENST00000370096.7:c.3137G=	ENSP00000359114.3:p.Gly1046=
ENST00000465209.1:n.145G=
ENST00000512756.5:c.2789G=	ENSP00000426533.1:p.Gly930=
ENST00000635193.1:c.2471G=
NM_001190709.1:c.3020G=	NP_001177638.1:p.Gly1007=
NM_001854.3:c.3137G=	NP_001845.3:p.Gly1046=
NM_080629.2:c.3173G=	NP_542196.2:p.Gly1058=
NM_080630.3:c.2789G=	NP_542197.3:p.Gly930=
XM_011540719.1:c.3137G=	XP_011539021.1:p.Gly1046=
XM_011540720.1:c.1370G=	XP_011539022.1:p.Gly457=
XM_011540721.1:c.725G=	XP_011539023.1:p.Gly242=
NR_134980.1:n.3471G=
XM_017000334.1:c.3290G=	XP_016855823.1:p.Gly1097=
XM_017000335.1:c.3284G=	XP_016855824.1:p.Gly1095=
XM_017000336.1:c.3290G=	XP_016855825.1:p.Gly1097=
XM_017000337.1:c.1688G=	XP_016855826.1:p.Gly563=
NM_001854.4:c.3137G= MANE Select	NP_001845.3:p.Gly1046=
NM_080630.4:c.2789G=	NP_542197.3:p.Gly930=
NR_134980.2:n.3497G=
NM_001190709.2:c.3020G=	NP_001177638.1:p.Gly1007=
NM_080629.3:c.3173G=	NP_542196.2:p.Gly1058=