Canonical Allele Identifier: CA2678434182

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35823662-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823663_35823664insGT , CM000668.2:g.35823663_35823664insGT	GRCh38
NC_000006.11:g.35791440_35791441insGT , CM000668.1:g.35791440_35791441insGT	GRCh37
NC_000006.10:g.35899418_35899419insGT	NCBI36
NG_012184.1:g.23370_23371insGT
NG_012184.2:g.23370_23371insGT
NG_012184.3:g.31458_31459insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*698_*699insGT MANE Select	ENSP00000353346.1:n.*698_*699insGT
ENST00000496656.2:n.578+3843_578+3844insGT
ENST00000651132.1:c.*698_*699insGT	ENSP00000498322.1:n.*698_*699insGT
ENST00000651676.1:c.*16+4200_*16+4201insGT	ENSP00000498699.1:n.*16+4200_*16+4201insGT
ENST00000651994.1:c.*778_*779insGT	ENSP00000498310.1:n.*778_*779insGT
ENST00000652718.1:c.508+4200_508+4201insGT	ENSP00000498866.1:n.508+4200_508+4201insGT
ENST00000360215.2:c.*698_*699insGT	ENSP00000353346.1:n.*698_*699insGT
ENST00000496656.1:n.812+3843_812+3844insGT
NM_182548.3:c.*698_*699insGT	NP_872354.1:n.*698_*699insGT
NM_182548.4:c.*698_*699insGT MANE Select	NP_872354.1:n.*698_*699insGT