Canonical Allele Identifier: CA1145984554

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979061G= , CM000663.2:g.102979061G=	GRCh38
NC_000001.10:g.103444617G= , CM000663.1:g.103444617G=	GRCh37
NC_000001.9:g.103217205G=	NCBI36
NG_008033.1:g.134436C=
NG_008033.2:g.134436C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2654C= MANE Select	ENSP00000359114.3:p.Thr885=
ENST00000353414.8:c.2537C=	ENSP00000302551.6:p.Thr846=
ENST00000358392.6:c.2690C=	ENSP00000351163.2:p.Thr897=
ENST00000370096.7:c.2654C=	ENSP00000359114.3:p.Thr885=
ENST00000512756.5:c.2306C=	ENSP00000426533.1:p.Thr769=
ENST00000635193.1:c.1988C=
NM_001190709.1:c.2537C=	NP_001177638.1:p.Thr846=
NM_001854.3:c.2654C=	NP_001845.3:p.Thr885=
NM_080629.2:c.2690C=	NP_542196.2:p.Thr897=
NM_080630.3:c.2306C=	NP_542197.3:p.Thr769=
XM_011540719.1:c.2654C=	XP_011539021.1:p.Thr885=
XM_011540720.1:c.887C=	XP_011539022.1:p.Thr296=
XM_011540721.1:c.242C=	XP_011539023.1:p.Thr81=
XR_946545.1:n.3068C=
NR_134980.1:n.2988C=
XM_017000334.1:c.2807C=	XP_016855823.1:p.Thr936=
XM_017000335.1:c.2801C=	XP_016855824.1:p.Thr934=
XM_017000336.1:c.2807C=	XP_016855825.1:p.Thr936=
XM_017000337.1:c.1205C=	XP_016855826.1:p.Thr402=
NM_001854.4:c.2654C= MANE Select	NP_001845.3:p.Thr885=
NM_080630.4:c.2306C=	NP_542197.3:p.Thr769=
NR_134980.2:n.3014C=
NM_001190709.2:c.2537C=	NP_001177638.1:p.Thr846=
NM_080629.3:c.2690C=	NP_542196.2:p.Thr897=