Canonical Allele Identifier: CA347656151
Gene: TMEM127 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.96931038C>T (hg19) chr2:g.96265300C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265300C>T , CM000664.2:g.96265300C>T GRCh38
NC_000002.11:g.96931038C>T , CM000664.1:g.96931038C>T GRCh37
NC_000002.10:g.96294765C>T NCBI36
NG_027695.1:g.5714G>A , LRG_528:g.5714G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.82G>A MANE Select ENSP00000258439.3:p.Glu28Lys
ENST00000258439.7:c.82G>A ENSP00000258439.2:p.Glu28Lys
ENST00000432959.1:c.82G>A ENSP00000416660.1:p.Glu28Lys
NM_001193304.2:c.82G>A NP_001180233.1:p.Glu28Lys
NM_017849.3:c.82G>A , LRG_528t1:c.82G>A NP_060319.1:p.Glu28Lys
NM_001193304.3:c.82G>A NP_001180233.1:p.Glu28Lys
NM_017849.4:c.82G>A MANE Select NP_060319.1:p.Glu28Lys
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