Canonical Allele Identifier: CA347651878

Gene: TMEM127

Linked Data

• dbSNP Id: rs751044006
• MyVariant Identifiers: chr2:g.96919643G>T (hg19) ; chr2:g.96253905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253905G>T , CM000664.2:g.96253905G>T	GRCh38
NC_000002.11:g.96919643G>T , CM000664.1:g.96919643G>T	GRCh37
NC_000002.10:g.96283370G>T	NCBI36
NG_027695.1:g.17109C>A , LRG_528:g.17109C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.620C>A MANE Select	ENSP00000258439.3:p.Ala207Glu
ENST00000258439.7:c.620C>A	ENSP00000258439.2:p.Ala207Glu
ENST00000432959.1:c.620C>A	ENSP00000416660.1:p.Ala207Glu
ENST00000435268.1:c.368C>A	ENSP00000411810.1:p.Ala123Glu
NM_001193304.2:c.620C>A	NP_001180233.1:p.Ala207Glu
NM_017849.3:c.620C>A , LRG_528t1:c.620C>A	NP_060319.1:p.Ala207Glu
XM_017004450.1:c.-299C>A	XP_016859939.1:n.-299C>A
XM_017004452.1:c.368C>A	XP_016859941.1:p.Ala123Glu
NM_001193304.3:c.620C>A	NP_001180233.1:p.Ala207Glu
NM_017849.4:c.620C>A MANE Select	NP_060319.1:p.Ala207Glu