Canonical Allele Identifier: CA1621066529

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814837_35814838delinsTG , CM000668.2:g.35814837_35814838delinsTG	GRCh38
NC_000006.11:g.35782614_35782615delinsTG , CM000668.1:g.35782614_35782615delinsTG	GRCh37
NC_000006.10:g.35890592_35890593delinsTG	NCBI36
NG_012184.1:g.14544_14545delinsTG
NG_012184.2:g.14544_14545delinsTG
NG_012184.3:g.22632_22633delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.649+55_649+56delinsTG MANE Select	ENSP00000353346.1:n.649+55_649+56delinsTG
ENST00000496656.2:n.428+55_428+56delinsTG
ENST00000651132.1:c.649+55_649+56delinsTG	ENSP00000498322.1:n.649+55_649+56delinsTG
ENST00000651676.1:c.649+55_649+56delinsTG	ENSP00000498699.1:n.649+55_649+56delinsTG
ENST00000651994.1:c.*70-4600_*70-4599delinsTG	ENSP00000498310.1:n.*70-4600_*70-4599delinsTG
ENST00000652718.1:c.481+55_481+56delinsTG	ENSP00000498866.1:n.481+55_481+56delinsTG
ENST00000360215.2:c.649+55_649+56delinsTG	ENSP00000353346.1:n.649+55_649+56delinsTG
ENST00000496656.1:n.428+55_428+56delinsTG
NM_182548.3:c.649+55_649+56delinsTG	NP_872354.1:n.649+55_649+56delinsTG
XM_011514403.1:c.649+55_649+56delinsTG	XP_011512705.1:n.649+55_649+56delinsTG
NM_182548.4:c.649+55_649+56delinsTG MANE Select	NP_872354.1:n.649+55_649+56delinsTG