Canonical Allele Identifier: CA650705097
Gene: LHFPL5 HGNC NCBI

Linked Data

COSMIC: COSN20451419
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823392_35823393insT , CM000668.2:g.35823392_35823393insT GRCh38
NC_000006.11:g.35791169_35791170insT , CM000668.1:g.35791169_35791170insT GRCh37
NC_000006.10:g.35899147_35899148insT NCBI36
NG_012184.1:g.23099_23100insT
NG_012184.2:g.23099_23100insT
NG_012184.3:g.31187_31188insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*427_*428insT MANE Select ENSP00000353346.1:n.*427_*428insT
ENST00000496656.2:n.578+3572_578+3573insT
ENST00000651132.1:c.*427_*428insT ENSP00000498322.1:n.*427_*428insT
ENST00000651676.1:c.*16+3929_*16+3930insT ENSP00000498699.1:n.*16+3929_*16+3930insT
ENST00000651994.1:c.*507_*508insT ENSP00000498310.1:n.*507_*508insT
ENST00000652718.1:c.508+3929_508+3930insT ENSP00000498866.1:n.508+3929_508+3930insT
ENST00000360215.2:c.*427_*428insT ENSP00000353346.1:n.*427_*428insT
ENST00000496656.1:n.812+3572_812+3573insT
NM_182548.3:c.*427_*428insT NP_872354.1:n.*427_*428insT
NM_182548.4:c.*427_*428insT MANE Select NP_872354.1:n.*427_*428insT
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