Canonical Allele Identifier: CA363784749
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs1181978085
gnomAD v3: 6-35805965-T-C
gnomAD v4: 6-35805965-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805965T>C , CM000668.2:g.35805965T>C GRCh38
NC_000006.11:g.35773742T>C , CM000668.1:g.35773742T>C GRCh37
NC_000006.10:g.35881720T>C NCBI36
NG_012184.1:g.5672T>C
NG_012184.2:g.5672T>C
NG_012184.3:g.13760T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360215.3:c.295T>C MANE Select ENSP00000353346.1:p.Phe99Leu
ENST00000651132.1:c.295T>C ENSP00000498322.1:p.Phe99Leu
ENST00000651676.1:c.295T>C ENSP00000498699.1:p.Phe99Leu
ENST00000651994.1:c.295T>C ENSP00000498310.1:p.Phe99Leu
ENST00000652718.1:c.127T>C ENSP00000498866.1:p.Phe43Leu
ENST00000360215.2:c.295T>C ENSP00000353346.1:p.Phe99Leu
NM_182548.3:c.295T>C NP_872354.1:p.Phe99Leu
XM_011514403.1:c.295T>C XP_011512705.1:p.Phe99Leu
NM_182548.4:c.295T>C MANE Select NP_872354.1:p.Phe99Leu