Canonical Allele Identifier: CA1621062626
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805957C= , CM000668.2:g.35805957C= GRCh38
NC_000006.11:g.35773734C= , CM000668.1:g.35773734C= GRCh37
NC_000006.10:g.35881712C= NCBI36
NG_012184.1:g.5664C=
NG_012184.2:g.5664C=
NG_012184.3:g.13752C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.287C= MANE Select ENSP00000353346.1:p.Thr96=
ENST00000651132.1:c.287C= ENSP00000498322.1:p.Thr96=
ENST00000651676.1:c.287C= ENSP00000498699.1:p.Thr96=
ENST00000651994.1:c.287C= ENSP00000498310.1:p.Thr96=
ENST00000652718.1:c.119C= ENSP00000498866.1:p.Thr40=
ENST00000360215.2:c.287C= ENSP00000353346.1:p.Thr96=
NM_182548.3:c.287C= NP_872354.1:p.Thr96=
XM_011514403.1:c.287C= XP_011512705.1:p.Thr96=
NM_182548.4:c.287C= MANE Select NP_872354.1:p.Thr96=