Canonical Allele Identifier: CA1272527008
Gene: TMEM127 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96265261_96265265delinsTAGAC , CM000664.2:g.96265261_96265265delinsTAGAC GRCh38
NC_000002.11:g.96930999_96931003delinsTAGAC , CM000664.1:g.96930999_96931003delinsTAGAC GRCh37
NC_000002.10:g.96294726_96294730delinsTAGAC NCBI36
NG_027695.1:g.5749_5753delinsGTCTA , LRG_528:g.5749_5753delinsGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258439.8:c.117_121delinsGTCTA MANE Select ENSP00000258439.3:p.Leu39=
ENST00000258439.7:c.117_121delinsGTCTA ENSP00000258439.2:p.Leu39=
ENST00000432959.1:c.117_121delinsGTCTA ENSP00000416660.1:p.Leu39=
NM_001193304.2:c.117_121delinsGTCTA NP_001180233.1:p.Leu39=
NM_017849.3:c.117_121delinsGTCTA , LRG_528t1:c.117_121delinsGTCTA NP_060319.1:p.Leu39=
NM_001193304.3:c.117_121delinsGTCTA NP_001180233.1:p.Leu39=
NM_017849.4:c.117_121delinsGTCTA MANE Select NP_060319.1:p.Leu39=
Search 100 bp 5'
Search 100 bp 3'