Canonical Allele Identifier: CA1272522483

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254839G= , CM000664.2:g.96254839G=	GRCh38
NC_000002.11:g.96920577G= , CM000664.1:g.96920577G=	GRCh37
NC_000002.10:g.96284304G=	NCBI36
NG_027695.1:g.16175C= , LRG_528:g.16175C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.403C= MANE Select	ENSP00000258439.3:p.Leu135=
ENST00000258439.7:c.403C=	ENSP00000258439.2:p.Leu135=
ENST00000432959.1:c.403C=	ENSP00000416660.1:p.Leu135=
ENST00000435268.1:c.151C=	ENSP00000411810.1:p.Leu51=
NM_001193304.2:c.403C=	NP_001180233.1:p.Leu135=
NM_017849.3:c.403C= , LRG_528t1:c.403C=	NP_060319.1:p.Leu135=
XM_017004450.1:c.-516C=	XP_016859939.1:n.-516C=
XM_017004452.1:c.151C=	XP_016859941.1:p.Leu51=
NM_001193304.3:c.403C=	NP_001180233.1:p.Leu135=
NM_017849.4:c.403C= MANE Select	NP_060319.1:p.Leu135=