Canonical Allele Identifier: CA1144081560

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979079C= , CM000663.2:g.102979079C=	GRCh38
NC_000001.10:g.103444635C= , CM000663.1:g.103444635C=	GRCh37
NC_000001.9:g.103217223C=	NCBI36
NG_008033.1:g.134418G=
NG_008033.2:g.134418G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2636G= MANE Select	ENSP00000359114.3:p.Arg879=
ENST00000353414.8:c.2519G=	ENSP00000302551.6:p.Arg840=
ENST00000358392.6:c.2672G=	ENSP00000351163.2:p.Arg891=
ENST00000370096.7:c.2636G=	ENSP00000359114.3:p.Arg879=
ENST00000512756.5:c.2288G=	ENSP00000426533.1:p.Arg763=
ENST00000635193.1:c.1970G=
NM_001190709.1:c.2519G=	NP_001177638.1:p.Arg840=
NM_001854.3:c.2636G=	NP_001845.3:p.Arg879=
NM_080629.2:c.2672G=	NP_542196.2:p.Arg891=
NM_080630.3:c.2288G=	NP_542197.3:p.Arg763=
XM_011540719.1:c.2636G=	XP_011539021.1:p.Arg879=
XM_011540720.1:c.869G=	XP_011539022.1:p.Arg290=
XM_011540721.1:c.224G=	XP_011539023.1:p.Arg75=
XR_946545.1:n.3050G=
NR_134980.1:n.2970G=
XM_017000334.1:c.2789G=	XP_016855823.1:p.Arg930=
XM_017000335.1:c.2783G=	XP_016855824.1:p.Arg928=
XM_017000336.1:c.2789G=	XP_016855825.1:p.Arg930=
XM_017000337.1:c.1187G=	XP_016855826.1:p.Arg396=
NM_001854.4:c.2636G= MANE Select	NP_001845.3:p.Arg879=
NM_080630.4:c.2288G=	NP_542197.3:p.Arg763=
NR_134980.2:n.2996G=
NM_001190709.2:c.2519G=	NP_001177638.1:p.Arg840=
NM_080629.3:c.2672G=	NP_542196.2:p.Arg891=