Canonical Allele Identifier: CA1143468222

Gene: TMCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165752166G= , CM000663.2:g.165752166G=	GRCh38
NC_000001.10:g.165721403G= , CM000663.1:g.165721403G=	GRCh37
NC_000001.9:g.163988027G=	NCBI36
NG_032004.1:g.21757C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367881.11:c.259C= MANE Select	ENSP00000356856.6:p.Arg87=
ENST00000465705.4:c.*90C=	ENSP00000463105.2:n.*90C=
ENST00000476143.7:c.*49C=	ENSP00000464127.2:n.*49C=
ENST00000367881.9:c.412C=	ENSP00000356856.5:p.Arg138=
ENST00000392129.10:c.259C=	ENSP00000375975.5:p.Arg87=
ENST00000464650.5:c.7C=	ENSP00000463951.1:p.Arg3=
ENST00000465705.3:c.*90C=	ENSP00000463105.1:n.*90C=
ENST00000476143.6:c.336C=
ENST00000481278.5:c.223C=	ENSP00000462300.1:p.Arg75=
ENST00000580248.5:c.7C=	ENSP00000462588.1:p.Arg3=
ENST00000612311.4:c.412C=	ENSP00000480514.1:p.Arg138=
NM_001256164.1:c.310C=	NP_001243093.1:p.Arg104=
NM_001256165.1:c.223C=	NP_001243094.1:p.Arg75=
NM_019026.4:c.412C=	NP_061899.2:p.Arg138=
NR_045818.1:n.353C=
NM_001366129.1:c.259C=	NP_001353058.1:p.Arg87=
NM_019026.5:c.259C=	NP_061899.3:p.Arg87=
NM_019026.6:c.259C= MANE Select	NP_061899.3:p.Arg87=