Canonical Allele Identifier: CA1272526984

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96265228C= , CM000664.2:g.96265228C=	GRCh38
NC_000002.11:g.96930966C= , CM000664.1:g.96930966C=	GRCh37
NC_000002.10:g.96294693C=	NCBI36
NG_027695.1:g.5786G= , LRG_528:g.5786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.154G= MANE Select	ENSP00000258439.3:p.Ala52=
ENST00000258439.7:c.154G=	ENSP00000258439.2:p.Ala52=
ENST00000432959.1:c.154G=	ENSP00000416660.1:p.Ala52=
NM_001193304.2:c.154G=	NP_001180233.1:p.Ala52=
NM_017849.3:c.154G= , LRG_528t1:c.154G=	NP_060319.1:p.Ala52=
NM_001193304.3:c.154G=	NP_001180233.1:p.Ala52=
NM_017849.4:c.154G= MANE Select	NP_060319.1:p.Ala52=