Canonical Allele Identifier: CA1272522153
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96254090G= , CM000664.2:g.96254090G= GRCh38
NC_000002.11:g.96919828G= , CM000664.1:g.96919828G= GRCh37
NC_000002.10:g.96283555G= NCBI36
NG_027695.1:g.16924C= , LRG_528:g.16924C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.435C= MANE Select ENSP00000258439.3:p.Gly145=
ENST00000258439.7:c.435C= ENSP00000258439.2:p.Gly145=
ENST00000432959.1:c.435C= ENSP00000416660.1:p.Gly145=
ENST00000435268.1:c.183C= ENSP00000411810.1:p.Gly61=
NM_001193304.2:c.435C= NP_001180233.1:p.Gly145=
NM_017849.3:c.435C= , LRG_528t1:c.435C= NP_060319.1:p.Gly145=
XM_017004450.1:c.-484C= XP_016859939.1:n.-484C=
XM_017004452.1:c.183C= XP_016859941.1:p.Gly61=
NM_001193304.3:c.435C= NP_001180233.1:p.Gly145=
NM_017849.4:c.435C= MANE Select NP_060319.1:p.Gly145=