Canonical Allele Identifier: CA1621068913
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823744G= , CM000668.2:g.35823744G= GRCh38
NC_000006.11:g.35791521G= , CM000668.1:g.35791521G= GRCh37
NC_000006.10:g.35899499G= NCBI36
NG_012184.1:g.23451G=
NG_012184.2:g.23451G=
NG_012184.3:g.31539G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*779G= MANE Select ENSP00000353346.1:n.*779G=
ENST00000496656.2:n.578+3924G=
ENST00000651132.1:c.*779G= ENSP00000498322.1:n.*779G=
ENST00000651676.1:c.*16+4281G= ENSP00000498699.1:n.*16+4281G=
ENST00000651994.1:c.*859G= ENSP00000498310.1:n.*859G=
ENST00000652718.1:c.508+4281G= ENSP00000498866.1:n.508+4281G=
ENST00000360215.2:c.*779G= ENSP00000353346.1:n.*779G=
ENST00000496656.1:n.812+3924G=
NM_182548.3:c.*779G= NP_872354.1:n.*779G=
NM_182548.4:c.*779G= MANE Select NP_872354.1:n.*779G=