Canonical Allele Identifier: CA450125220
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782405G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814628G>C , CM000668.2:g.35814628G>C GRCh38
NC_000006.11:g.35782405G>C , CM000668.1:g.35782405G>C GRCh37
NC_000006.10:g.35890383G>C NCBI36
NG_012184.1:g.14335G>C
NG_012184.2:g.14335G>C
NG_012184.3:g.22423G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.495G>C MANE Select ENSP00000353346.1:p.Thr165=
ENST00000496656.2:n.274G>C
ENST00000651132.1:c.495G>C ENSP00000498322.1:p.Thr165=
ENST00000651676.1:c.495G>C ENSP00000498699.1:p.Thr165=
ENST00000651994.1:c.*70-4809G>C ENSP00000498310.1:n.*70-4809G>C
ENST00000652718.1:c.327G>C ENSP00000498866.1:p.Thr109=
ENST00000360215.2:c.495G>C ENSP00000353346.1:p.Thr165=
ENST00000496656.1:n.274G>C
NM_182548.3:c.495G>C NP_872354.1:p.Thr165=
XM_011514403.1:c.495G>C XP_011512705.1:p.Thr165=
NM_182548.4:c.495G>C MANE Select NP_872354.1:p.Thr165=