Canonical Allele Identifier: CA1621068908
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823735T= , CM000668.2:g.35823735T= GRCh38
NC_000006.11:g.35791512T= , CM000668.1:g.35791512T= GRCh37
NC_000006.10:g.35899490T= NCBI36
NG_012184.1:g.23442T=
NG_012184.2:g.23442T=
NG_012184.3:g.31530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*770T= MANE Select ENSP00000353346.1:n.*770T=
ENST00000496656.2:n.578+3915T=
ENST00000651132.1:c.*770T= ENSP00000498322.1:n.*770T=
ENST00000651676.1:c.*16+4272T= ENSP00000498699.1:n.*16+4272T=
ENST00000651994.1:c.*850T= ENSP00000498310.1:n.*850T=
ENST00000652718.1:c.508+4272T= ENSP00000498866.1:n.508+4272T=
ENST00000360215.2:c.*770T= ENSP00000353346.1:n.*770T=
ENST00000496656.1:n.812+3915T=
NM_182548.3:c.*770T= NP_872354.1:n.*770T=
NM_182548.4:c.*770T= MANE Select NP_872354.1:n.*770T=