Canonical Allele Identifier: CA3774351
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs776088980
gnomAD v2: 6-35773628-T-C
gnomAD v4: 6-35805851-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805851T>C , CM000668.2:g.35805851T>C GRCh38
NC_000006.11:g.35773628T>C , CM000668.1:g.35773628T>C GRCh37
NC_000006.10:g.35881606T>C NCBI36
NG_012184.1:g.5558T>C
NG_012184.2:g.5558T>C
NG_012184.3:g.13646T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.181T>C MANE Select ENSP00000353346.1:p.Tyr61His
ENST00000651132.1:c.181T>C ENSP00000498322.1:p.Tyr61His
ENST00000651676.1:c.181T>C ENSP00000498699.1:p.Tyr61His
ENST00000651994.1:c.181T>C ENSP00000498310.1:p.Tyr61His
ENST00000652718.1:c.13T>C ENSP00000498866.1:p.Tyr5His
ENST00000360215.2:c.181T>C ENSP00000353346.1:p.Tyr61His
NM_182548.3:c.181T>C NP_872354.1:p.Tyr61His
XM_011514403.1:c.181T>C XP_011512705.1:p.Tyr61His
NM_182548.4:c.181T>C MANE Select NP_872354.1:p.Tyr61His