Canonical Allele Identifier: CA1272527384
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1684413421
gnomAD v4: 2-96265890-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265890G>A , CM000664.2:g.96265890G>A GRCh38
NC_000002.11:g.96931628G>A , CM000664.1:g.96931628G>A GRCh37
NC_000002.10:g.96295355G>A NCBI36
NG_027695.1:g.5124C>T , LRG_528:g.5124C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-153C>T MANE Select ENSP00000258439.3:n.-153C>T
ENST00000258439.7:c.-153C>T ENSP00000258439.2:n.-153C>T
ENST00000432959.1:c.-130C>T ENSP00000416660.1:n.-130C>T
NM_001193304.2:c.-130C>T NP_001180233.1:n.-130C>T
NM_017849.3:c.-153C>T , LRG_528t1:c.-153C>T NP_060319.1:n.-153C>T
NM_001193304.3:c.-130C>T NP_001180233.1:n.-130C>T
NM_017849.4:c.-153C>T MANE Select NP_060319.1:n.-153C>T
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