Canonical Allele Identifier: CA1185271903

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978725C= , CM000663.2:g.102978725C=	GRCh38
NC_000001.10:g.103444281C= , CM000663.1:g.103444281C=	GRCh37
NC_000001.9:g.103216869C=	NCBI36
NG_008033.1:g.134772G=
NG_008033.2:g.134772G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2737G= MANE Select	ENSP00000359114.3:p.Gly913=
ENST00000353414.8:c.2620G=	ENSP00000302551.6:p.Gly874=
ENST00000358392.6:c.2773G=	ENSP00000351163.2:p.Gly925=
ENST00000370096.7:c.2737G=	ENSP00000359114.3:p.Gly913=
ENST00000512756.5:c.2389G=	ENSP00000426533.1:p.Gly797=
ENST00000635193.1:c.2071G=
NM_001190709.1:c.2620G=	NP_001177638.1:p.Gly874=
NM_001854.3:c.2737G=	NP_001845.3:p.Gly913=
NM_080629.2:c.2773G=	NP_542196.2:p.Gly925=
NM_080630.3:c.2389G=	NP_542197.3:p.Gly797=
XM_011540719.1:c.2737G=	XP_011539021.1:p.Gly913=
XM_011540720.1:c.970G=	XP_011539022.1:p.Gly324=
XM_011540721.1:c.325G=	XP_011539023.1:p.Gly109=
XR_946545.1:n.3151G=
NR_134980.1:n.3071G=
XM_017000334.1:c.2890G=	XP_016855823.1:p.Gly964=
XM_017000335.1:c.2884G=	XP_016855824.1:p.Gly962=
XM_017000336.1:c.2890G=	XP_016855825.1:p.Gly964=
XM_017000337.1:c.1288G=	XP_016855826.1:p.Gly430=
NM_001854.4:c.2737G= MANE Select	NP_001845.3:p.Gly913=
NM_080630.4:c.2389G=	NP_542197.3:p.Gly797=
NR_134980.2:n.3097G=
NM_001190709.2:c.2620G=	NP_001177638.1:p.Gly874=
NM_080629.3:c.2773G=	NP_542196.2:p.Gly925=