Canonical Allele Identifier: CA1185272070

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979088G= , CM000663.2:g.102979088G=	GRCh38
NC_000001.10:g.103444644G= , CM000663.1:g.103444644G=	GRCh37
NC_000001.9:g.103217232G=	NCBI36
NG_008033.1:g.134409C=
NG_008033.2:g.134409C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2627C= MANE Select	ENSP00000359114.3:p.Pro876=
ENST00000353414.8:c.2510C=	ENSP00000302551.6:p.Pro837=
ENST00000358392.6:c.2663C=	ENSP00000351163.2:p.Pro888=
ENST00000370096.7:c.2627C=	ENSP00000359114.3:p.Pro876=
ENST00000512756.5:c.2279C=	ENSP00000426533.1:p.Pro760=
ENST00000635193.1:c.1961C=
NM_001190709.1:c.2510C=	NP_001177638.1:p.Pro837=
NM_001854.3:c.2627C=	NP_001845.3:p.Pro876=
NM_080629.2:c.2663C=	NP_542196.2:p.Pro888=
NM_080630.3:c.2279C=	NP_542197.3:p.Pro760=
XM_011540719.1:c.2627C=	XP_011539021.1:p.Pro876=
XM_011540720.1:c.860C=	XP_011539022.1:p.Pro287=
XM_011540721.1:c.215C=	XP_011539023.1:p.Pro72=
XR_946545.1:n.3041C=
NR_134980.1:n.2961C=
XM_017000334.1:c.2780C=	XP_016855823.1:p.Pro927=
XM_017000335.1:c.2774C=	XP_016855824.1:p.Pro925=
XM_017000336.1:c.2780C=	XP_016855825.1:p.Pro927=
XM_017000337.1:c.1178C=	XP_016855826.1:p.Pro393=
NM_001854.4:c.2627C= MANE Select	NP_001845.3:p.Pro876=
NM_080630.4:c.2279C=	NP_542197.3:p.Pro760=
NR_134980.2:n.2987C=
NM_001190709.2:c.2510C=	NP_001177638.1:p.Pro837=
NM_080629.3:c.2663C=	NP_542196.2:p.Pro888=