Canonical Allele Identifier: CA1087852032
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1768909438

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823425del , CM000668.2:g.35823425del GRCh38
NC_000006.11:g.35791202del , CM000668.1:g.35791202del GRCh37
NC_000006.10:g.35899180del NCBI36
NG_012184.1:g.23132del
NG_012184.2:g.23132del
NG_012184.3:g.31220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*460del MANE Select ENSP00000353346.1:n.*460del
ENST00000496656.2:n.578+3605del
ENST00000651132.1:c.*460del ENSP00000498322.1:n.*460del
ENST00000651676.1:c.*16+3962del ENSP00000498699.1:n.*16+3962del
ENST00000651994.1:c.*540del ENSP00000498310.1:n.*540del
ENST00000652718.1:c.508+3962del ENSP00000498866.1:n.508+3962del
ENST00000360215.2:c.*460del ENSP00000353346.1:n.*460del
ENST00000496656.1:n.812+3605del
NM_182548.3:c.*460del NP_872354.1:n.*460del
NM_182548.4:c.*460del MANE Select NP_872354.1:n.*460del