Canonical Allele Identifier: CA1621066511
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35814791C= , CM000668.2:g.35814791C= GRCh38
NC_000006.11:g.35782568C= , CM000668.1:g.35782568C= GRCh37
NC_000006.10:g.35890546C= NCBI36
NG_012184.1:g.14498C=
NG_012184.2:g.14498C=
NG_012184.3:g.22586C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.649+9C= MANE Select ENSP00000353346.1:n.649+9C=
ENST00000496656.2:n.428+9C=
ENST00000651132.1:c.649+9C= ENSP00000498322.1:n.649+9C=
ENST00000651676.1:c.649+9C= ENSP00000498699.1:n.649+9C=
ENST00000651994.1:c.*70-4646C= ENSP00000498310.1:n.*70-4646C=
ENST00000652718.1:c.481+9C= ENSP00000498866.1:n.481+9C=
ENST00000360215.2:c.649+9C= ENSP00000353346.1:n.649+9C=
ENST00000496656.1:n.428+9C=
NM_182548.3:c.649+9C= NP_872354.1:n.649+9C=
XM_011514403.1:c.649+9C= XP_011512705.1:n.649+9C=
NM_182548.4:c.649+9C= MANE Select NP_872354.1:n.649+9C=