Canonical Allele Identifier: CA1143765332

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979082G= , CM000663.2:g.102979082G=	GRCh38
NC_000001.10:g.103444638G= , CM000663.1:g.103444638G=	GRCh37
NC_000001.9:g.103217226G=	NCBI36
NG_008033.1:g.134415C=
NG_008033.2:g.134415C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2633C= MANE Select	ENSP00000359114.3:p.Pro878=
ENST00000353414.8:c.2516C=	ENSP00000302551.6:p.Pro839=
ENST00000358392.6:c.2669C=	ENSP00000351163.2:p.Pro890=
ENST00000370096.7:c.2633C=	ENSP00000359114.3:p.Pro878=
ENST00000512756.5:c.2285C=	ENSP00000426533.1:p.Pro762=
ENST00000635193.1:c.1967C=
NM_001190709.1:c.2516C=	NP_001177638.1:p.Pro839=
NM_001854.3:c.2633C=	NP_001845.3:p.Pro878=
NM_080629.2:c.2669C=	NP_542196.2:p.Pro890=
NM_080630.3:c.2285C=	NP_542197.3:p.Pro762=
XM_011540719.1:c.2633C=	XP_011539021.1:p.Pro878=
XM_011540720.1:c.866C=	XP_011539022.1:p.Pro289=
XM_011540721.1:c.221C=	XP_011539023.1:p.Pro74=
XR_946545.1:n.3047C=
NR_134980.1:n.2967C=
XM_017000334.1:c.2786C=	XP_016855823.1:p.Pro929=
XM_017000335.1:c.2780C=	XP_016855824.1:p.Pro927=
XM_017000336.1:c.2786C=	XP_016855825.1:p.Pro929=
XM_017000337.1:c.1184C=	XP_016855826.1:p.Pro395=
NM_001854.4:c.2633C= MANE Select	NP_001845.3:p.Pro878=
NM_080630.4:c.2285C=	NP_542197.3:p.Pro762=
NR_134980.2:n.2993C=
NM_001190709.2:c.2516C=	NP_001177638.1:p.Pro839=
NM_080629.3:c.2669C=	NP_542196.2:p.Pro890=