Canonical Allele Identifier: CA3774416
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs770093293
gnomAD v2: 6-35782353-A-G
gnomAD v4: 6-35814576-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814576A>G , CM000668.2:g.35814576A>G GRCh38
NC_000006.11:g.35782353A>G , CM000668.1:g.35782353A>G GRCh37
NC_000006.10:g.35890331A>G NCBI36
NG_012184.1:g.14283A>G
NG_012184.2:g.14283A>G
NG_012184.3:g.22371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.443A>G MANE Select ENSP00000353346.1:p.Tyr148Cys
ENST00000496656.2:n.222A>G
ENST00000651132.1:c.443A>G ENSP00000498322.1:p.Tyr148Cys
ENST00000651676.1:c.443A>G ENSP00000498699.1:p.Tyr148Cys
ENST00000651994.1:c.*70-4861A>G ENSP00000498310.1:n.*70-4861A>G
ENST00000652718.1:c.275A>G ENSP00000498866.1:p.Tyr92Cys
ENST00000360215.2:c.443A>G ENSP00000353346.1:p.Tyr148Cys
ENST00000496656.1:n.222A>G
NM_182548.3:c.443A>G NP_872354.1:p.Tyr148Cys
XM_011514403.1:c.443A>G XP_011512705.1:p.Tyr148Cys
NM_182548.4:c.443A>G MANE Select NP_872354.1:p.Tyr148Cys