Canonical Allele Identifier: CA450125076
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782324C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814547C>A , CM000668.2:g.35814547C>A GRCh38
NC_000006.11:g.35782324C>A , CM000668.1:g.35782324C>A GRCh37
NC_000006.10:g.35890302C>A NCBI36
NG_012184.1:g.14254C>A
NG_012184.2:g.14254C>A
NG_012184.3:g.22342C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360215.3:c.414C>A MANE Select ENSP00000353346.1:p.Ala138=
ENST00000496656.2:n.193C>A
ENST00000651132.1:c.414C>A ENSP00000498322.1:p.Ala138=
ENST00000651676.1:c.414C>A ENSP00000498699.1:p.Ala138=
ENST00000651994.1:c.*70-4890C>A ENSP00000498310.1:n.*70-4890C>A
ENST00000652718.1:c.246C>A ENSP00000498866.1:p.Ala82=
ENST00000360215.2:c.414C>A ENSP00000353346.1:p.Ala138=
ENST00000496656.1:n.193C>A
NM_182548.3:c.414C>A NP_872354.1:p.Ala138=
XM_011514403.1:c.414C>A XP_011512705.1:p.Ala138=
NM_182548.4:c.414C>A MANE Select NP_872354.1:p.Ala138=