Canonical Allele Identifier: CA1185272074

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979099T= , CM000663.2:g.102979099T=	GRCh38
NC_000001.10:g.103444655T= , CM000663.1:g.103444655T=	GRCh37
NC_000001.9:g.103217243T=	NCBI36
NG_008033.1:g.134398A=
NG_008033.2:g.134398A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2616A= MANE Select	ENSP00000359114.3:p.Val872=
ENST00000353414.8:c.2499A=	ENSP00000302551.6:p.Val833=
ENST00000358392.6:c.2652A=	ENSP00000351163.2:p.Val884=
ENST00000370096.7:c.2616A=	ENSP00000359114.3:p.Val872=
ENST00000512756.5:c.2268A=	ENSP00000426533.1:p.Val756=
ENST00000635193.1:c.1950A=
NM_001190709.1:c.2499A=	NP_001177638.1:p.Val833=
NM_001854.3:c.2616A=	NP_001845.3:p.Val872=
NM_080629.2:c.2652A=	NP_542196.2:p.Val884=
NM_080630.3:c.2268A=	NP_542197.3:p.Val756=
XM_011540719.1:c.2616A=	XP_011539021.1:p.Val872=
XM_011540720.1:c.849A=	XP_011539022.1:p.Val283=
XM_011540721.1:c.204A=	XP_011539023.1:p.Val68=
XR_946545.1:n.3030A=
NR_134980.1:n.2950A=
XM_017000334.1:c.2769A=	XP_016855823.1:p.Val923=
XM_017000335.1:c.2763A=	XP_016855824.1:p.Val921=
XM_017000336.1:c.2769A=	XP_016855825.1:p.Val923=
XM_017000337.1:c.1167A=	XP_016855826.1:p.Val389=
NM_001854.4:c.2616A= MANE Select	NP_001845.3:p.Val872=
NM_080630.4:c.2268A=	NP_542197.3:p.Val756=
NR_134980.2:n.2976A=
NM_001190709.2:c.2499A=	NP_001177638.1:p.Val833=
NM_080629.3:c.2652A=	NP_542196.2:p.Val884=