Canonical Allele Identifier: CA450125088
Gene: LHFPL5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35782333A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814556A>G , CM000668.2:g.35814556A>G GRCh38
NC_000006.11:g.35782333A>G , CM000668.1:g.35782333A>G GRCh37
NC_000006.10:g.35890311A>G NCBI36
NG_012184.1:g.14263A>G
NG_012184.2:g.14263A>G
NG_012184.3:g.22351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.423A>G MANE Select ENSP00000353346.1:p.Leu141=
ENST00000496656.2:n.202A>G
ENST00000651132.1:c.423A>G ENSP00000498322.1:p.Leu141=
ENST00000651676.1:c.423A>G ENSP00000498699.1:p.Leu141=
ENST00000651994.1:c.*70-4881A>G ENSP00000498310.1:n.*70-4881A>G
ENST00000652718.1:c.255A>G ENSP00000498866.1:p.Leu85=
ENST00000360215.2:c.423A>G ENSP00000353346.1:p.Leu141=
ENST00000496656.1:n.202A>G
NM_182548.3:c.423A>G NP_872354.1:p.Leu141=
XM_011514403.1:c.423A>G XP_011512705.1:p.Leu141=
NM_182548.4:c.423A>G MANE Select NP_872354.1:p.Leu141=