Canonical Allele Identifier: CA1272522489

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254847G= , CM000664.2:g.96254847G=	GRCh38
NC_000002.11:g.96920585G= , CM000664.1:g.96920585G=	GRCh37
NC_000002.10:g.96284312G=	NCBI36
NG_027695.1:g.16167C= , LRG_528:g.16167C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.395C= MANE Select	ENSP00000258439.3:p.Ala132=
ENST00000258439.7:c.395C=	ENSP00000258439.2:p.Ala132=
ENST00000432959.1:c.395C=	ENSP00000416660.1:p.Ala132=
ENST00000435268.1:c.143C=	ENSP00000411810.1:p.Ala48=
NM_001193304.2:c.395C=	NP_001180233.1:p.Ala132=
NM_017849.3:c.395C= , LRG_528t1:c.395C=	NP_060319.1:p.Ala132=
XM_017004450.1:c.-524C=	XP_016859939.1:n.-524C=
XM_017004452.1:c.143C=	XP_016859941.1:p.Ala48=
NM_001193304.3:c.395C=	NP_001180233.1:p.Ala132=
NM_017849.4:c.395C= MANE Select	NP_060319.1:p.Ala132=