Canonical Allele Identifier: CA1185258719

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946919C= , CM000663.2:g.102946919C=	GRCh38
NC_000001.10:g.103412475C= , CM000663.1:g.103412475C=	GRCh37
NC_000001.9:g.103185063C=	NCBI36
NG_008033.1:g.166578G=
NG_008033.2:g.166578G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3206G= MANE Select	ENSP00000359114.3:p.Gly1069=
ENST00000353414.8:c.3089G=	ENSP00000302551.6:p.Gly1030=
ENST00000358392.6:c.3242G=	ENSP00000351163.2:p.Gly1081=
ENST00000370096.7:c.3206G=	ENSP00000359114.3:p.Gly1069=
ENST00000512756.5:c.2858G=	ENSP00000426533.1:p.Gly953=
ENST00000635193.1:c.2540G=
NM_001190709.1:c.3089G=	NP_001177638.1:p.Gly1030=
NM_001854.3:c.3206G=	NP_001845.3:p.Gly1069=
NM_080629.2:c.3242G=	NP_542196.2:p.Gly1081=
NM_080630.3:c.2858G=	NP_542197.3:p.Gly953=
XM_011540719.1:c.3206G=	XP_011539021.1:p.Gly1069=
XM_011540720.1:c.1439G=	XP_011539022.1:p.Gly480=
XM_011540721.1:c.794G=	XP_011539023.1:p.Gly265=
NR_134980.1:n.3540G=
XM_017000334.1:c.3359G=	XP_016855823.1:p.Gly1120=
XM_017000335.1:c.3353G=	XP_016855824.1:p.Gly1118=
XM_017000336.1:c.3359G=	XP_016855825.1:p.Gly1120=
XM_017000337.1:c.1757G=	XP_016855826.1:p.Gly586=
NM_001854.4:c.3206G= MANE Select	NP_001845.3:p.Gly1069=
NM_080630.4:c.2858G=	NP_542197.3:p.Gly953=
NR_134980.2:n.3566G=
NM_001190709.2:c.3089G=	NP_001177638.1:p.Gly1030=
NM_080629.3:c.3242G=	NP_542196.2:p.Gly1081=