Canonical Allele Identifier: CA427808071
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1573969264
MyVariant Identifiers: chr2:g.96919756G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254018G>A , CM000664.2:g.96254018G>A GRCh38
NC_000002.11:g.96919756G>A , CM000664.1:g.96919756G>A GRCh37
NC_000002.10:g.96283483G>A NCBI36
NG_027695.1:g.16996C>T , LRG_528:g.16996C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.507C>T MANE Select ENSP00000258439.3:p.Val169=
ENST00000258439.7:c.507C>T ENSP00000258439.2:p.Val169=
ENST00000432959.1:c.507C>T ENSP00000416660.1:p.Val169=
ENST00000435268.1:c.255C>T ENSP00000411810.1:p.Val85=
NM_001193304.2:c.507C>T NP_001180233.1:p.Val169=
NM_017849.3:c.507C>T , LRG_528t1:c.507C>T NP_060319.1:p.Val169=
XM_017004450.1:c.-412C>T XP_016859939.1:n.-412C>T
XM_017004452.1:c.255C>T XP_016859941.1:p.Val85=
NM_001193304.3:c.507C>T NP_001180233.1:p.Val169=
NM_017849.4:c.507C>T MANE Select NP_060319.1:p.Val169=