Canonical Allele Identifier: CA1621068722
Gene: LHFPL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823442T= , CM000668.2:g.35823442T= GRCh38
NC_000006.11:g.35791219T= , CM000668.1:g.35791219T= GRCh37
NC_000006.10:g.35899197T= NCBI36
NG_012184.1:g.23149T=
NG_012184.2:g.23149T=
NG_012184.3:g.31237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*477T= MANE Select ENSP00000353346.1:n.*477T=
ENST00000496656.2:n.578+3622T=
ENST00000651132.1:c.*477T= ENSP00000498322.1:n.*477T=
ENST00000651676.1:c.*16+3979T= ENSP00000498699.1:n.*16+3979T=
ENST00000651994.1:c.*557T= ENSP00000498310.1:n.*557T=
ENST00000652718.1:c.508+3979T= ENSP00000498866.1:n.508+3979T=
ENST00000360215.2:c.*477T= ENSP00000353346.1:n.*477T=
ENST00000496656.1:n.812+3622T=
NM_182548.3:c.*477T= NP_872354.1:n.*477T=
NM_182548.4:c.*477T= MANE Select NP_872354.1:n.*477T=