Canonical Allele Identifier: CA450125097
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782346C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814569C>T , CM000668.2:g.35814569C>T GRCh38
NC_000006.11:g.35782346C>T , CM000668.1:g.35782346C>T GRCh37
NC_000006.10:g.35890324C>T NCBI36
NG_012184.1:g.14276C>T
NG_012184.2:g.14276C>T
NG_012184.3:g.22364C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.436C>T MANE Select ENSP00000353346.1:p.Leu146=
ENST00000496656.2:n.215C>T
ENST00000651132.1:c.436C>T ENSP00000498322.1:p.Leu146=
ENST00000651676.1:c.436C>T ENSP00000498699.1:p.Leu146=
ENST00000651994.1:c.*70-4868C>T ENSP00000498310.1:n.*70-4868C>T
ENST00000652718.1:c.268C>T ENSP00000498866.1:p.Leu90=
ENST00000360215.2:c.436C>T ENSP00000353346.1:p.Leu146=
ENST00000496656.1:n.215C>T
NM_182548.3:c.436C>T NP_872354.1:p.Leu146=
XM_011514403.1:c.436C>T XP_011512705.1:p.Leu146=
NM_182548.4:c.436C>T MANE Select NP_872354.1:p.Leu146=