Canonical Allele Identifier: CA1621062629
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35805965T= , CM000668.2:g.35805965T= GRCh38
NC_000006.11:g.35773742T= , CM000668.1:g.35773742T= GRCh37
NC_000006.10:g.35881720T= NCBI36
NG_012184.1:g.5672T=
NG_012184.2:g.5672T=
NG_012184.3:g.13760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.295T= MANE Select ENSP00000353346.1:p.Phe99=
ENST00000651132.1:c.295T= ENSP00000498322.1:p.Phe99=
ENST00000651676.1:c.295T= ENSP00000498699.1:p.Phe99=
ENST00000651994.1:c.295T= ENSP00000498310.1:p.Phe99=
ENST00000652718.1:c.127T= ENSP00000498866.1:p.Phe43=
ENST00000360215.2:c.295T= ENSP00000353346.1:p.Phe99=
NM_182548.3:c.295T= NP_872354.1:p.Phe99=
XM_011514403.1:c.295T= XP_011512705.1:p.Phe99=
NM_182548.4:c.295T= MANE Select NP_872354.1:p.Phe99=