Canonical Allele Identifier: CA137310767
Gene: LHFPL5 HGNC NCBI

Linked Data

dbSNP Id: rs781647481
gnomAD v4: 6-35814738-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814738G>C , CM000668.2:g.35814738G>C GRCh38
NC_000006.11:g.35782515G>C , CM000668.1:g.35782515G>C GRCh37
NC_000006.10:g.35890493G>C NCBI36
NG_012184.1:g.14445G>C
NG_012184.2:g.14445G>C
NG_012184.3:g.22533G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.605G>C MANE Select ENSP00000353346.1:p.Arg202Pro
ENST00000496656.2:n.384G>C
ENST00000651132.1:c.605G>C ENSP00000498322.1:p.Arg202Pro
ENST00000651676.1:c.605G>C ENSP00000498699.1:p.Arg202Pro
ENST00000651994.1:c.*70-4699G>C ENSP00000498310.1:n.*70-4699G>C
ENST00000652718.1:c.437G>C ENSP00000498866.1:p.Arg146Pro
ENST00000360215.2:c.605G>C ENSP00000353346.1:p.Arg202Pro
ENST00000496656.1:n.384G>C
NM_182548.3:c.605G>C NP_872354.1:p.Arg202Pro
XM_011514403.1:c.605G>C XP_011512705.1:p.Arg202Pro
NM_182548.4:c.605G>C MANE Select NP_872354.1:p.Arg202Pro