Canonical Allele Identifier: CA1139885973

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102888582A= , CM000663.2:g.102888582A=	GRCh38
NC_000001.10:g.103354138A= , CM000663.1:g.103354138A=	GRCh37
NC_000001.9:g.103126726A=	NCBI36
NG_008033.1:g.224915T=
NG_008033.2:g.224915T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.4603T= MANE Select	NP_001845.3:p.Ser1535=
ENST00000370096.9:c.4603T= MANE Select	ENSP00000359114.3:p.Ser1535=
NM_001190709.1:c.4486T=	NP_001177638.1:p.Ser1496=
NM_001190709.2:c.4486T=	NP_001177638.1:p.Ser1496=
NM_001854.3:c.4603T=	NP_001845.3:p.Ser1535=
NM_080629.2:c.4639T=	NP_542196.2:p.Ser1547=
NM_080629.3:c.4639T=	NP_542196.2:p.Ser1547=
NM_080630.3:c.4255T=	NP_542197.3:p.Ser1419=
NM_080630.4:c.4255T=	NP_542197.3:p.Ser1419=
NR_134980.1:n.4937T=
NR_134980.2:n.4963T=
ENST00000353414.8:c.4486T=	ENSP00000302551.6:p.Ser1496=
ENST00000358392.6:c.4639T=	ENSP00000351163.2:p.Ser1547=
ENST00000370096.7:c.4603T=	ENSP00000359114.3:p.Ser1535=
ENST00000512756.5:c.4255T=	ENSP00000426533.1:p.Ser1419=
ENST00000635193.1:c.3937T=
XM_011540720.1:c.2836T=	XP_011539022.1:p.Ser946=
XM_011540721.1:c.2191T=	XP_011539023.1:p.Ser731=
XM_017000334.1:c.4756T=	XP_016855823.1:p.Ser1586=
XM_017000335.1:c.4750T=	XP_016855824.1:p.Ser1584=
XM_017000337.1:c.3154T=	XP_016855826.1:p.Ser1052=