Canonical Allele Identifier: CA450125232
Gene: LHFPL5 HGNC NCBI

Linked Data

gnomAD v4: 6-35814646-C-A
MyVariant Identifiers: chr6:g.35782423C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814646C>A , CM000668.2:g.35814646C>A GRCh38
NC_000006.11:g.35782423C>A , CM000668.1:g.35782423C>A GRCh37
NC_000006.10:g.35890401C>A NCBI36
NG_012184.1:g.14353C>A
NG_012184.2:g.14353C>A
NG_012184.3:g.22441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.513C>A MANE Select ENSP00000353346.1:p.Gly171=
ENST00000496656.2:n.292C>A
ENST00000651132.1:c.513C>A ENSP00000498322.1:p.Gly171=
ENST00000651676.1:c.513C>A ENSP00000498699.1:p.Gly171=
ENST00000651994.1:c.*70-4791C>A ENSP00000498310.1:n.*70-4791C>A
ENST00000652718.1:c.345C>A ENSP00000498866.1:p.Gly115=
ENST00000360215.2:c.513C>A ENSP00000353346.1:p.Gly171=
ENST00000496656.1:n.292C>A
NM_182548.3:c.513C>A NP_872354.1:p.Gly171=
XM_011514403.1:c.513C>A XP_011512705.1:p.Gly171=
NM_182548.4:c.513C>A MANE Select NP_872354.1:p.Gly171=