Canonical Allele Identifier: CA1272522067
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96253928G= , CM000664.2:g.96253928G= GRCh38
NC_000002.11:g.96919666G= , CM000664.1:g.96919666G= GRCh37
NC_000002.10:g.96283393G= NCBI36
NG_027695.1:g.17086C= , LRG_528:g.17086C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.597C= MANE Select ENSP00000258439.3:p.Tyr199=
ENST00000258439.7:c.597C= ENSP00000258439.2:p.Tyr199=
ENST00000432959.1:c.597C= ENSP00000416660.1:p.Tyr199=
ENST00000435268.1:c.345C= ENSP00000411810.1:p.Tyr115=
NM_001193304.2:c.597C= NP_001180233.1:p.Tyr199=
NM_017849.3:c.597C= , LRG_528t1:c.597C= NP_060319.1:p.Tyr199=
XM_017004450.1:c.-322C= XP_016859939.1:n.-322C=
XM_017004452.1:c.345C= XP_016859941.1:p.Tyr115=
NM_001193304.3:c.597C= NP_001180233.1:p.Tyr199=
NM_017849.4:c.597C= MANE Select NP_060319.1:p.Tyr199=