Canonical Allele Identifier: CA1185271905

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978728G= , CM000663.2:g.102978728G=	GRCh38
NC_000001.10:g.103444284G= , CM000663.1:g.103444284G=	GRCh37
NC_000001.9:g.103216872G=	NCBI36
NG_008033.1:g.134769C=
NG_008033.2:g.134769C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2734C= MANE Select	ENSP00000359114.3:p.Pro912=
ENST00000353414.8:c.2617C=	ENSP00000302551.6:p.Pro873=
ENST00000358392.6:c.2770C=	ENSP00000351163.2:p.Pro924=
ENST00000370096.7:c.2734C=	ENSP00000359114.3:p.Pro912=
ENST00000512756.5:c.2386C=	ENSP00000426533.1:p.Pro796=
ENST00000635193.1:c.2068C=
NM_001190709.1:c.2617C=	NP_001177638.1:p.Pro873=
NM_001854.3:c.2734C=	NP_001845.3:p.Pro912=
NM_080629.2:c.2770C=	NP_542196.2:p.Pro924=
NM_080630.3:c.2386C=	NP_542197.3:p.Pro796=
XM_011540719.1:c.2734C=	XP_011539021.1:p.Pro912=
XM_011540720.1:c.967C=	XP_011539022.1:p.Pro323=
XM_011540721.1:c.322C=	XP_011539023.1:p.Pro108=
XR_946545.1:n.3148C=
NR_134980.1:n.3068C=
XM_017000334.1:c.2887C=	XP_016855823.1:p.Pro963=
XM_017000335.1:c.2881C=	XP_016855824.1:p.Pro961=
XM_017000336.1:c.2887C=	XP_016855825.1:p.Pro963=
XM_017000337.1:c.1285C=	XP_016855826.1:p.Pro429=
NM_001854.4:c.2734C= MANE Select	NP_001845.3:p.Pro912=
NM_080630.4:c.2386C=	NP_542197.3:p.Pro796=
NR_134980.2:n.3094C=
NM_001190709.2:c.2617C=	NP_001177638.1:p.Pro873=
NM_080629.3:c.2770C=	NP_542196.2:p.Pro924=