Canonical Allele Identifier: CA3081421667

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102998317C= , CM000663.2:g.102998317C=	GRCh38
NC_000001.10:g.103463873C= , CM000663.1:g.103463873C=	GRCh37
NC_000001.9:g.103236461C=	NCBI36
NG_008033.1:g.115180G=
NG_008033.2:g.115180G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.2189G= MANE Select	NP_001845.3:p.Gly730=
ENST00000370096.9:c.2189G= MANE Select	ENSP00000359114.3:p.Gly730=
NM_001190709.1:c.2072G=	NP_001177638.1:p.Gly691=
NM_001190709.2:c.2072G=	NP_001177638.1:p.Gly691=
NM_001854.3:c.2189G=	NP_001845.3:p.Gly730=
NM_080629.2:c.2225G=	NP_542196.2:p.Gly742=
NM_080629.3:c.2225G=	NP_542196.2:p.Gly742=
NM_080630.3:c.1841G=	NP_542197.3:p.Gly614=
NM_080630.4:c.1841G=	NP_542197.3:p.Gly614=
NR_134980.1:n.2507G=
NR_134980.2:n.2533G=
ENST00000353414.8:c.2072G=	ENSP00000302551.6:p.Gly691=
ENST00000358392.6:c.2225G=	ENSP00000351163.2:p.Gly742=
ENST00000370096.7:c.2189G=	ENSP00000359114.3:p.Gly730=
ENST00000512756.5:c.1841G=	ENSP00000426533.1:p.Gly614=
ENST00000635193.1:c.1507G=
XM_011540719.1:c.2189G=	XP_011539021.1:p.Gly730=
XM_011540720.1:c.422G=	XP_011539022.1:p.Gly141=
XM_011540721.1:c.-240G=	XP_011539023.1:n.-240G=
XM_017000334.1:c.2342G=	XP_016855823.1:p.Gly781=
XM_017000335.1:c.2336G=	XP_016855824.1:p.Gly779=
XM_017000336.1:c.2342G=	XP_016855825.1:p.Gly781=
XM_017000337.1:c.740G=	XP_016855826.1:p.Gly247=
XR_946545.1:n.2587G=