Canonical Allele Identifier: CA1185271895

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978708T= , CM000663.2:g.102978708T=	GRCh38
NC_000001.10:g.103444264T= , CM000663.1:g.103444264T=	GRCh37
NC_000001.9:g.103216852T=	NCBI36
NG_008033.1:g.134789A=
NG_008033.2:g.134789A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2754A= MANE Select	ENSP00000359114.3:p.Arg918=
ENST00000353414.8:c.2637A=	ENSP00000302551.6:p.Arg879=
ENST00000358392.6:c.2790A=	ENSP00000351163.2:p.Arg930=
ENST00000370096.7:c.2754A=	ENSP00000359114.3:p.Arg918=
ENST00000512756.5:c.2406A=	ENSP00000426533.1:p.Arg802=
ENST00000635193.1:c.2088A=
NM_001190709.1:c.2637A=	NP_001177638.1:p.Arg879=
NM_001854.3:c.2754A=	NP_001845.3:p.Arg918=
NM_080629.2:c.2790A=	NP_542196.2:p.Arg930=
NM_080630.3:c.2406A=	NP_542197.3:p.Arg802=
XM_011540719.1:c.2754A=	XP_011539021.1:p.Arg918=
XM_011540720.1:c.987A=	XP_011539022.1:p.Arg329=
XM_011540721.1:c.342A=	XP_011539023.1:p.Arg114=
XR_946545.1:n.3168A=
NR_134980.1:n.3088A=
XM_017000334.1:c.2907A=	XP_016855823.1:p.Arg969=
XM_017000335.1:c.2901A=	XP_016855824.1:p.Arg967=
XM_017000336.1:c.2907A=	XP_016855825.1:p.Arg969=
XM_017000337.1:c.1305A=	XP_016855826.1:p.Arg435=
NM_001854.4:c.2754A= MANE Select	NP_001845.3:p.Arg918=
NM_080630.4:c.2406A=	NP_542197.3:p.Arg802=
NR_134980.2:n.3114A=
NM_001190709.2:c.2637A=	NP_001177638.1:p.Arg879=
NM_080629.3:c.2790A=	NP_542196.2:p.Arg930=