Canonical Allele Identifier: CA1272522064
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253924T= , CM000664.2:g.96253924T= GRCh38
NC_000002.11:g.96919662T= , CM000664.1:g.96919662T= GRCh37
NC_000002.10:g.96283389T= NCBI36
NG_027695.1:g.17090A= , LRG_528:g.17090A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.601A= MANE Select ENSP00000258439.3:p.Thr201=
ENST00000258439.7:c.601A= ENSP00000258439.2:p.Thr201=
ENST00000432959.1:c.601A= ENSP00000416660.1:p.Thr201=
ENST00000435268.1:c.349A= ENSP00000411810.1:p.Thr117=
NM_001193304.2:c.601A= NP_001180233.1:p.Thr201=
NM_017849.3:c.601A= , LRG_528t1:c.601A= NP_060319.1:p.Thr201=
XM_017004450.1:c.-318A= XP_016859939.1:n.-318A=
XM_017004452.1:c.349A= XP_016859941.1:p.Thr117=
NM_001193304.3:c.601A= NP_001180233.1:p.Thr201=
NM_017849.4:c.601A= MANE Select NP_060319.1:p.Thr201=