Canonical Allele Identifier: CA2751314149
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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