Canonical Allele Identifier: CA3774369
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs746718708
gnomAD v2: 6-35773717-C-A
gnomAD v4: 6-35805940-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805940C>A , CM000668.2:g.35805940C>A GRCh38
NC_000006.11:g.35773717C>A , CM000668.1:g.35773717C>A GRCh37
NC_000006.10:g.35881695C>A NCBI36
NG_012184.1:g.5647C>A
NG_012184.2:g.5647C>A
NG_012184.3:g.13735C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.270C>A MANE Select ENSP00000353346.1:p.Pro90=
ENST00000651132.1:c.270C>A ENSP00000498322.1:p.Pro90=
ENST00000651676.1:c.270C>A ENSP00000498699.1:p.Pro90=
ENST00000651994.1:c.270C>A ENSP00000498310.1:p.Pro90=
ENST00000652718.1:c.102C>A ENSP00000498866.1:p.Pro34=
ENST00000360215.2:c.270C>A ENSP00000353346.1:p.Pro90=
NM_182548.3:c.270C>A NP_872354.1:p.Pro90=
XM_011514403.1:c.270C>A XP_011512705.1:p.Pro90=
NM_182548.4:c.270C>A MANE Select NP_872354.1:p.Pro90=