Canonical Allele Identifier: CA2497029681
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823858_35823859delinsAT , CM000668.2:g.35823858_35823859delinsAT GRCh38
NC_000006.11:g.35791635_35791636delinsAT , CM000668.1:g.35791635_35791636delinsAT GRCh37
NC_000006.10:g.35899613_35899614delinsAT NCBI36
NG_012184.1:g.23565_23566delinsAT
NG_012184.2:g.23565_23566delinsAT
NG_012184.3:g.31653_31654delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*893_*894delinsAT MANE Select ENSP00000353346.1:n.*893_*894delinsAT
ENST00000496656.2:n.578+4038_578+4039delinsAT
ENST00000651132.1:c.*893_*894delinsAT ENSP00000498322.1:n.*893_*894delinsAT
ENST00000651676.1:c.*16+4395_*16+4396delinsAT ENSP00000498699.1:n.*16+4395_*16+4396delinsAT
ENST00000651994.1:c.*973_*974delinsAT ENSP00000498310.1:n.*973_*974delinsAT
ENST00000652718.1:c.508+4395_508+4396delinsAT ENSP00000498866.1:n.508+4395_508+4396delinsAT
ENST00000360215.2:c.*893_*894delinsAT ENSP00000353346.1:n.*893_*894delinsAT
ENST00000496656.1:n.812+4038_812+4039delinsAT
NM_182548.3:c.*893_*894delinsAT NP_872354.1:n.*893_*894delinsAT
NM_182548.4:c.*893_*894delinsAT MANE Select NP_872354.1:n.*893_*894delinsAT