Canonical Allele Identifier: CA1141729864

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102961893T= , CM000663.2:g.102961893T=	GRCh38
NC_000001.10:g.103427449T= , CM000663.1:g.103427449T=	GRCh37
NC_000001.9:g.103200037T=	NCBI36
NG_008033.1:g.151604A=
NG_008033.2:g.151604A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3141A= MANE Select	ENSP00000359114.3:p.Glu1047=
ENST00000353414.8:c.3024A=	ENSP00000302551.6:p.Glu1008=
ENST00000358392.6:c.3177A=	ENSP00000351163.2:p.Glu1059=
ENST00000370096.7:c.3141A=	ENSP00000359114.3:p.Glu1047=
ENST00000465209.1:n.149A=
ENST00000512756.5:c.2793A=	ENSP00000426533.1:p.Glu931=
ENST00000635193.1:c.2475A=
NM_001190709.1:c.3024A=	NP_001177638.1:p.Glu1008=
NM_001854.3:c.3141A=	NP_001845.3:p.Glu1047=
NM_080629.2:c.3177A=	NP_542196.2:p.Glu1059=
NM_080630.3:c.2793A=	NP_542197.3:p.Glu931=
XM_011540719.1:c.3141A=	XP_011539021.1:p.Glu1047=
XM_011540720.1:c.1374A=	XP_011539022.1:p.Glu458=
XM_011540721.1:c.729A=	XP_011539023.1:p.Glu243=
NR_134980.1:n.3475A=
XM_017000334.1:c.3294A=	XP_016855823.1:p.Glu1098=
XM_017000335.1:c.3288A=	XP_016855824.1:p.Glu1096=
XM_017000336.1:c.3294A=	XP_016855825.1:p.Glu1098=
XM_017000337.1:c.1692A=	XP_016855826.1:p.Glu564=
NM_001854.4:c.3141A= MANE Select	NP_001845.3:p.Glu1047=
NM_080630.4:c.2793A=	NP_542197.3:p.Glu931=
NR_134980.2:n.3501A=
NM_001190709.2:c.3024A=	NP_001177638.1:p.Glu1008=
NM_080629.3:c.3177A=	NP_542196.2:p.Glu1059=