Canonical Allele Identifier: CA1272521466

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96252410G= , CM000664.2:g.96252410G=	GRCh38
NC_000002.11:g.96918148G= , CM000664.1:g.96918148G=	GRCh37
NC_000002.10:g.96281875G=	NCBI36
NG_027695.1:g.18604C= , LRG_528:g.18604C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*1398C= MANE Select	ENSP00000258439.3:n.*1398C=
ENST00000258439.7:c.*1398C=	ENSP00000258439.2:n.*1398C=
ENST00000432959.1:c.*1398C=	ENSP00000416660.1:n.*1398C=
NM_001193304.2:c.*1398C=	NP_001180233.1:n.*1398C=
NM_017849.3:c.*1398C= , LRG_528t1:c.*1398C=	NP_060319.1:n.*1398C=
XM_017004450.1:c.*699C=	XP_016859939.1:n.*699C=
XM_017004452.1:c.*1398C=	XP_016859941.1:n.*1398C=
NM_001193304.3:c.*1398C=	NP_001180233.1:n.*1398C=
NM_017849.4:c.*1398C= MANE Select	NP_060319.1:n.*1398C=