Canonical Allele Identifier: CA2678434156
Gene: LHFPL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35823636_35823637insT , CM000668.2:g.35823636_35823637insT GRCh38
NC_000006.11:g.35791413_35791414insT , CM000668.1:g.35791413_35791414insT GRCh37
NC_000006.10:g.35899391_35899392insT NCBI36
NG_012184.1:g.23343_23344insT
NG_012184.2:g.23343_23344insT
NG_012184.3:g.31431_31432insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360215.3:c.*671_*672insT MANE Select ENSP00000353346.1:n.*671_*672insT
ENST00000496656.2:n.578+3816_578+3817insT
ENST00000651132.1:c.*671_*672insT ENSP00000498322.1:n.*671_*672insT
ENST00000651676.1:c.*16+4173_*16+4174insT ENSP00000498699.1:n.*16+4173_*16+4174insT
ENST00000651994.1:c.*751_*752insT ENSP00000498310.1:n.*751_*752insT
ENST00000652718.1:c.508+4173_508+4174insT ENSP00000498866.1:n.508+4173_508+4174insT
ENST00000360215.2:c.*671_*672insT ENSP00000353346.1:n.*671_*672insT
ENST00000496656.1:n.812+3816_812+3817insT
NM_182548.3:c.*671_*672insT NP_872354.1:n.*671_*672insT
NM_182548.4:c.*671_*672insT MANE Select NP_872354.1:n.*671_*672insT