Canonical Allele Identifier: CA1272521106
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1022594114
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251632C>T , CM000664.2:g.96251632C>T GRCh38
NC_000002.11:g.96917370C>T , CM000664.1:g.96917370C>T GRCh37
NC_000002.10:g.96281097C>T NCBI36
NG_027695.1:g.19382G>A , LRG_528:g.19382G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2176G>A MANE Select ENSP00000258439.3:n.*2176G>A
ENST00000258439.7:c.*2176G>A ENSP00000258439.2:n.*2176G>A
NM_001193304.2:c.*2176G>A NP_001180233.1:n.*2176G>A
NM_017849.3:c.*2176G>A , LRG_528t1:c.*2176G>A NP_060319.1:n.*2176G>A
XM_017004450.1:c.*1477G>A XP_016859939.1:n.*1477G>A
XM_017004452.1:c.*2176G>A XP_016859941.1:n.*2176G>A
NM_001193304.3:c.*2176G>A NP_001180233.1:n.*2176G>A
NM_017849.4:c.*2176G>A MANE Select NP_060319.1:n.*2176G>A
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