Canonical Allele Identifier: CA3774437
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs767971303
gnomAD v4: 6-35814684-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814684T>A , CM000668.2:g.35814684T>A GRCh38
NC_000006.11:g.35782461T>A , CM000668.1:g.35782461T>A GRCh37
NC_000006.10:g.35890439T>A NCBI36
NG_012184.1:g.14391T>A
NG_012184.2:g.14391T>A
NG_012184.3:g.22479T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.551T>A MANE Select ENSP00000353346.1:p.Leu184His
ENST00000496656.2:n.330T>A
ENST00000651132.1:c.551T>A ENSP00000498322.1:p.Leu184His
ENST00000651676.1:c.551T>A ENSP00000498699.1:p.Leu184His
ENST00000651994.1:c.*70-4753T>A ENSP00000498310.1:n.*70-4753T>A
ENST00000652718.1:c.383T>A ENSP00000498866.1:p.Leu128His
ENST00000360215.2:c.551T>A ENSP00000353346.1:p.Leu184His
ENST00000496656.1:n.330T>A
NM_182548.3:c.551T>A NP_872354.1:p.Leu184His
XM_011514403.1:c.551T>A XP_011512705.1:p.Leu184His
NM_182548.4:c.551T>A MANE Select NP_872354.1:p.Leu184His