Canonical Allele Identifier: CA1185272062

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979057T= , CM000663.2:g.102979057T=	GRCh38
NC_000001.10:g.103444613T= , CM000663.1:g.103444613T=	GRCh37
NC_000001.9:g.103217201T=	NCBI36
NG_008033.1:g.134440A=
NG_008033.2:g.134440A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2655+3A= MANE Select	ENSP00000359114.3:n.2655+3A=
ENST00000353414.8:c.2538+3A=	ENSP00000302551.6:n.2538+3A=
ENST00000358392.6:c.2691+3A=	ENSP00000351163.2:n.2691+3A=
ENST00000370096.7:c.2655+3A=	ENSP00000359114.3:n.2655+3A=
ENST00000512756.5:c.2307+3A=	ENSP00000426533.1:n.2307+3A=
ENST00000635193.1:c.1989+3A=
NM_001190709.1:c.2538+3A=	NP_001177638.1:n.2538+3A=
NM_001854.3:c.2655+3A=	NP_001845.3:n.2655+3A=
NM_080629.2:c.2691+3A=	NP_542196.2:n.2691+3A=
NM_080630.3:c.2307+3A=	NP_542197.3:n.2307+3A=
XM_011540719.1:c.2655+3A=	XP_011539021.1:n.2655+3A=
XM_011540720.1:c.888+3A=	XP_011539022.1:n.888+3A=
XM_011540721.1:c.243+3A=	XP_011539023.1:n.243+3A=
XR_946545.1:n.3069+3A=
NR_134980.1:n.2989+3A=
XM_017000334.1:c.2808+3A=	XP_016855823.1:n.2808+3A=
XM_017000335.1:c.2802+3A=	XP_016855824.1:n.2802+3A=
XM_017000336.1:c.2808+3A=	XP_016855825.1:n.2808+3A=
XM_017000337.1:c.1206+3A=	XP_016855826.1:n.1206+3A=
NM_001854.4:c.2655+3A= MANE Select	NP_001845.3:n.2655+3A=
NM_080630.4:c.2307+3A=	NP_542197.3:n.2307+3A=
NR_134980.2:n.3015+3A=
NM_001190709.2:c.2538+3A=	NP_001177638.1:n.2538+3A=
NM_080629.3:c.2691+3A=	NP_542196.2:n.2691+3A=