Canonical Allele Identifier: CA1621068951
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823826T= , CM000668.2:g.35823826T= GRCh38
NC_000006.11:g.35791603T= , CM000668.1:g.35791603T= GRCh37
NC_000006.10:g.35899581T= NCBI36
NG_012184.1:g.23533T=
NG_012184.2:g.23533T=
NG_012184.3:g.31621T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*861T= MANE Select ENSP00000353346.1:n.*861T=
ENST00000496656.2:n.578+4006T=
ENST00000651132.1:c.*861T= ENSP00000498322.1:n.*861T=
ENST00000651676.1:c.*16+4363T= ENSP00000498699.1:n.*16+4363T=
ENST00000651994.1:c.*941T= ENSP00000498310.1:n.*941T=
ENST00000652718.1:c.508+4363T= ENSP00000498866.1:n.508+4363T=
ENST00000360215.2:c.*861T= ENSP00000353346.1:n.*861T=
ENST00000496656.1:n.812+4006T=
NM_182548.3:c.*861T= NP_872354.1:n.*861T=
NM_182548.4:c.*861T= MANE Select NP_872354.1:n.*861T=