Canonical Allele Identifier: CA1185258692

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946897G= , CM000663.2:g.102946897G=	GRCh38
NC_000001.10:g.103412453G= , CM000663.1:g.103412453G=	GRCh37
NC_000001.9:g.103185041G=	NCBI36
NG_008033.1:g.166600C=
NG_008033.2:g.166600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3228C= MANE Select	ENSP00000359114.3:p.Arg1076=
ENST00000353414.8:c.3111C=	ENSP00000302551.6:p.Arg1037=
ENST00000358392.6:c.3264C=	ENSP00000351163.2:p.Arg1088=
ENST00000370096.7:c.3228C=	ENSP00000359114.3:p.Arg1076=
ENST00000512756.5:c.2880C=	ENSP00000426533.1:p.Arg960=
ENST00000635193.1:c.2562C=
NM_001190709.1:c.3111C=	NP_001177638.1:p.Arg1037=
NM_001854.3:c.3228C=	NP_001845.3:p.Arg1076=
NM_080629.2:c.3264C=	NP_542196.2:p.Arg1088=
NM_080630.3:c.2880C=	NP_542197.3:p.Arg960=
XM_011540719.1:c.3228C=	XP_011539021.1:p.Arg1076=
XM_011540720.1:c.1461C=	XP_011539022.1:p.Arg487=
XM_011540721.1:c.816C=	XP_011539023.1:p.Arg272=
NR_134980.1:n.3562C=
XM_017000334.1:c.3381C=	XP_016855823.1:p.Arg1127=
XM_017000335.1:c.3375C=	XP_016855824.1:p.Arg1125=
XM_017000336.1:c.3381C=	XP_016855825.1:p.Arg1127=
XM_017000337.1:c.1779C=	XP_016855826.1:p.Arg593=
NM_001854.4:c.3228C= MANE Select	NP_001845.3:p.Arg1076=
NM_080630.4:c.2880C=	NP_542197.3:p.Arg960=
NR_134980.2:n.3588C=
NM_001190709.2:c.3111C=	NP_001177638.1:p.Arg1037=
NM_080629.3:c.3264C=	NP_542196.2:p.Arg1088=