Canonical Allele Identifier: CA1185284681

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103008514C= , CM000663.2:g.103008514C=	GRCh38
NC_000001.10:g.103474070C= , CM000663.1:g.103474070C=	GRCh37
NC_000001.9:g.103246658C=	NCBI36
NG_008033.1:g.104983G=
NG_008033.2:g.104983G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.1632G= MANE Select	ENSP00000359114.3:p.Gly544=
ENST00000461720.6:c.1785G=	ENSP00000494909.1:p.Gly595=
ENST00000644186.1:c.1632G=	ENSP00000493821.1:p.Gly544=
ENST00000645458.1:c.1632G=	ENSP00000494179.1:p.Gly544=
ENST00000647280.1:c.1632G=	ENSP00000494583.1:p.Gly544=
ENST00000353414.8:c.1515G=	ENSP00000302551.6:p.Gly505=
ENST00000358392.6:c.1668G=	ENSP00000351163.2:p.Gly556=
ENST00000370096.7:c.1632G=	ENSP00000359114.3:p.Gly544=
ENST00000427239.5:c.1668G=	ENSP00000408640.1:p.Gly556=
ENST00000512756.5:c.1284G=	ENSP00000426533.1:p.Gly428=
ENST00000635193.1:c.950G=
NM_001190709.1:c.1515G=	NP_001177638.1:p.Gly505=
NM_001854.3:c.1632G=	NP_001845.3:p.Gly544=
NM_080629.2:c.1668G=	NP_542196.2:p.Gly556=
NM_080630.3:c.1284G=	NP_542197.3:p.Gly428=
XM_011540719.1:c.1632G=	XP_011539021.1:p.Gly544=
XM_011540720.1:c.-85+162G=	XP_011539022.1:n.-85+162G=
XM_011540721.1:c.-797G=	XP_011539023.1:n.-797G=
XR_946545.1:n.2030G=
NR_134980.1:n.1950G=
XM_017000334.1:c.1785G=	XP_016855823.1:p.Gly595=
XM_017000335.1:c.1779G=	XP_016855824.1:p.Gly593=
XM_017000336.1:c.1785G=	XP_016855825.1:p.Gly595=
XM_017000337.1:c.183G=	XP_016855826.1:p.Gly61=
NM_001854.4:c.1632G= MANE Select	NP_001845.3:p.Gly544=
NM_080630.4:c.1284G=	NP_542197.3:p.Gly428=
NR_134980.2:n.1976G=
NM_001190709.2:c.1515G=	NP_001177638.1:p.Gly505=
NM_080629.3:c.1668G=	NP_542196.2:p.Gly556=