Canonical Allele Identifier: CA2660177916
Gene: TMEM127 HGNC NCBI

Linked Data

gnomAD v4: 2-96265894-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265894T>G , CM000664.2:g.96265894T>G GRCh38
NC_000002.11:g.96931632T>G , CM000664.1:g.96931632T>G GRCh37
NC_000002.10:g.96295359T>G NCBI36
NG_027695.1:g.5120A>C , LRG_528:g.5120A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.-157A>C MANE Select ENSP00000258439.3:n.-157A>C
ENST00000258439.7:c.-157A>C ENSP00000258439.2:n.-157A>C
ENST00000432959.1:c.-134A>C ENSP00000416660.1:n.-134A>C
NM_001193304.2:c.-134A>C NP_001180233.1:n.-134A>C
NM_017849.3:c.-157A>C , LRG_528t1:c.-157A>C NP_060319.1:n.-157A>C
NM_001193304.3:c.-134A>C NP_001180233.1:n.-134A>C
NM_017849.4:c.-157A>C MANE Select NP_060319.1:n.-157A>C
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