Canonical Allele Identifier: CA1621066513
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814795C= , CM000668.2:g.35814795C= GRCh38
NC_000006.11:g.35782572C= , CM000668.1:g.35782572C= GRCh37
NC_000006.10:g.35890550C= NCBI36
NG_012184.1:g.14502C=
NG_012184.2:g.14502C=
NG_012184.3:g.22590C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.649+13C= MANE Select ENSP00000353346.1:n.649+13C=
ENST00000496656.2:n.428+13C=
ENST00000651132.1:c.649+13C= ENSP00000498322.1:n.649+13C=
ENST00000651676.1:c.649+13C= ENSP00000498699.1:n.649+13C=
ENST00000651994.1:c.*70-4642C= ENSP00000498310.1:n.*70-4642C=
ENST00000652718.1:c.481+13C= ENSP00000498866.1:n.481+13C=
ENST00000360215.2:c.649+13C= ENSP00000353346.1:n.649+13C=
ENST00000496656.1:n.428+13C=
NM_182548.3:c.649+13C= NP_872354.1:n.649+13C=
XM_011514403.1:c.649+13C= XP_011512705.1:n.649+13C=
NM_182548.4:c.649+13C= MANE Select NP_872354.1:n.649+13C=