Canonical Allele Identifier: CA2660177912
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96265888-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265888C>A , CM000664.2:g.96265888C>A GRCh38
NC_000002.11:g.96931626C>A , CM000664.1:g.96931626C>A GRCh37
NC_000002.10:g.96295353C>A NCBI36
NG_027695.1:g.5126G>T , LRG_528:g.5126G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-151G>T MANE Select ENSP00000258439.3:n.-151G>T
ENST00000258439.7:c.-151G>T ENSP00000258439.2:n.-151G>T
ENST00000432959.1:c.-128G>T ENSP00000416660.1:n.-128G>T
NM_001193304.2:c.-128G>T NP_001180233.1:n.-128G>T
NM_017849.3:c.-151G>T , LRG_528t1:c.-151G>T NP_060319.1:n.-151G>T
NM_001193304.3:c.-128G>T NP_001180233.1:n.-128G>T
NM_017849.4:c.-151G>T MANE Select NP_060319.1:n.-151G>T
Search 100 bp 5'
Search 100 bp 3'