Canonical Allele Identifier: CA895768593
Gene: TMEM127 HGNC NCBI

Linked Data

dbSNP Id: rs1190575201
MyVariant Identifiers: chr2:g.96916745del (hg19) chr2:g.96251007del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96251007del , CM000664.2:g.96251007del GRCh38
NC_000002.11:g.96916745del , CM000664.1:g.96916745del GRCh37
NC_000002.10:g.96280472del NCBI36
NG_027695.1:g.20007del , LRG_528:g.20007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.*2801del MANE Select ENSP00000258439.3:n.*2801del
ENST00000258439.7:c.*2801del ENSP00000258439.2:n.*2801del
NM_001193304.2:c.*2801del NP_001180233.1:n.*2801del
NM_017849.3:c.*2801del , LRG_528t1:c.*2801del NP_060319.1:n.*2801del
XM_017004450.1:c.*2102del XP_016859939.1:n.*2102del
XM_017004452.1:c.*2801del XP_016859941.1:n.*2801del
NM_001193304.3:c.*2801del NP_001180233.1:n.*2801del
NM_017849.4:c.*2801del MANE Select NP_060319.1:n.*2801del
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