Canonical Allele Identifier: CA2660177921
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96265899-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265899C>T , CM000664.2:g.96265899C>T GRCh38
NC_000002.11:g.96931637C>T , CM000664.1:g.96931637C>T GRCh37
NC_000002.10:g.96295364C>T NCBI36
NG_027695.1:g.5115G>A , LRG_528:g.5115G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-162G>A MANE Select ENSP00000258439.3:n.-162G>A
ENST00000258439.7:c.-162G>A ENSP00000258439.2:n.-162G>A
ENST00000432959.1:c.-139G>A ENSP00000416660.1:n.-139G>A
NM_001193304.2:c.-139G>A NP_001180233.1:n.-139G>A
NM_017849.3:c.-162G>A , LRG_528t1:c.-162G>A NP_060319.1:n.-162G>A
NM_001193304.3:c.-139G>A NP_001180233.1:n.-139G>A
NM_017849.4:c.-162G>A MANE Select NP_060319.1:n.-162G>A
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