Canonical Allele Identifier: CA1185258643

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946862T= , CM000663.2:g.102946862T=	GRCh38
NC_000001.10:g.103412418T= , CM000663.1:g.103412418T=	GRCh37
NC_000001.9:g.103185006T=	NCBI36
NG_008033.1:g.166635A=
NG_008033.2:g.166635A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3263A= MANE Select	ENSP00000359114.3:p.Glu1088=
ENST00000353414.8:c.3146A=	ENSP00000302551.6:p.Glu1049=
ENST00000358392.6:c.3299A=	ENSP00000351163.2:p.Glu1100=
ENST00000370096.7:c.3263A=	ENSP00000359114.3:p.Glu1088=
ENST00000512756.5:c.2915A=	ENSP00000426533.1:p.Glu972=
ENST00000635193.1:c.2597A=
NM_001190709.1:c.3146A=	NP_001177638.1:p.Glu1049=
NM_001854.3:c.3263A=	NP_001845.3:p.Glu1088=
NM_080629.2:c.3299A=	NP_542196.2:p.Glu1100=
NM_080630.3:c.2915A=	NP_542197.3:p.Glu972=
XM_011540719.1:c.3263A=	XP_011539021.1:p.Glu1088=
XM_011540720.1:c.1496A=	XP_011539022.1:p.Glu499=
XM_011540721.1:c.851A=	XP_011539023.1:p.Glu284=
NR_134980.1:n.3597A=
XM_017000334.1:c.3416A=	XP_016855823.1:p.Glu1139=
XM_017000335.1:c.3410A=	XP_016855824.1:p.Glu1137=
XM_017000336.1:c.3416A=	XP_016855825.1:p.Glu1139=
XM_017000337.1:c.1814A=	XP_016855826.1:p.Glu605=
NM_001854.4:c.3263A= MANE Select	NP_001845.3:p.Glu1088=
NM_080630.4:c.2915A=	NP_542197.3:p.Glu972=
NR_134980.2:n.3623A=
NM_001190709.2:c.3146A=	NP_001177638.1:p.Glu1049=
NM_080629.3:c.3299A=	NP_542196.2:p.Glu1100=