Canonical Allele Identifier: CA450125213
Gene: LHFPL5 HGNC NCBI

Linked Data

gnomAD v4: 6-35814610-C-T
MyVariant Identifiers: chr6:g.35782387C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814610C>T , CM000668.2:g.35814610C>T GRCh38
NC_000006.11:g.35782387C>T , CM000668.1:g.35782387C>T GRCh37
NC_000006.10:g.35890365C>T NCBI36
NG_012184.1:g.14317C>T
NG_012184.2:g.14317C>T
NG_012184.3:g.22405C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.477C>T MANE Select ENSP00000353346.1:p.Arg159=
ENST00000496656.2:n.256C>T
ENST00000651132.1:c.477C>T ENSP00000498322.1:p.Arg159=
ENST00000651676.1:c.477C>T ENSP00000498699.1:p.Arg159=
ENST00000651994.1:c.*70-4827C>T ENSP00000498310.1:n.*70-4827C>T
ENST00000652718.1:c.309C>T ENSP00000498866.1:p.Arg103=
ENST00000360215.2:c.477C>T ENSP00000353346.1:p.Arg159=
ENST00000496656.1:n.256C>T
NM_182548.3:c.477C>T NP_872354.1:p.Arg159=
XM_011514403.1:c.477C>T XP_011512705.1:p.Arg159=
NM_182548.4:c.477C>T MANE Select NP_872354.1:p.Arg159=