Canonical Allele Identifier: CA3081421676

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102998325A= , CM000663.2:g.102998325A=	GRCh38
NC_000001.10:g.103463881A= , CM000663.1:g.103463881A=	GRCh37
NC_000001.9:g.103236469A=	NCBI36
NG_008033.1:g.115172T=
NG_008033.2:g.115172T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.2181T= MANE Select	NP_001845.3:p.Gly727=
ENST00000370096.9:c.2181T= MANE Select	ENSP00000359114.3:p.Gly727=
NM_001190709.1:c.2064T=	NP_001177638.1:p.Gly688=
NM_001190709.2:c.2064T=	NP_001177638.1:p.Gly688=
NM_001854.3:c.2181T=	NP_001845.3:p.Gly727=
NM_080629.2:c.2217T=	NP_542196.2:p.Gly739=
NM_080629.3:c.2217T=	NP_542196.2:p.Gly739=
NM_080630.3:c.1833T=	NP_542197.3:p.Gly611=
NM_080630.4:c.1833T=	NP_542197.3:p.Gly611=
NR_134980.1:n.2499T=
NR_134980.2:n.2525T=
ENST00000353414.8:c.2064T=	ENSP00000302551.6:p.Gly688=
ENST00000358392.6:c.2217T=	ENSP00000351163.2:p.Gly739=
ENST00000370096.7:c.2181T=	ENSP00000359114.3:p.Gly727=
ENST00000512756.5:c.1833T=	ENSP00000426533.1:p.Gly611=
ENST00000635193.1:c.1499T=
XM_011540719.1:c.2181T=	XP_011539021.1:p.Gly727=
XM_011540720.1:c.414T=	XP_011539022.1:p.Gly138=
XM_011540721.1:c.-248T=	XP_011539023.1:n.-248T=
XM_017000334.1:c.2334T=	XP_016855823.1:p.Gly778=
XM_017000335.1:c.2328T=	XP_016855824.1:p.Gly776=
XM_017000336.1:c.2334T=	XP_016855825.1:p.Gly778=
XM_017000337.1:c.732T=	XP_016855826.1:p.Gly244=
XR_946545.1:n.2579T=