Canonical Allele Identifier: CA2678433177

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35814809-CCCCTGCCTGGAGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814815_35814827del , CM000668.2:g.35814815_35814827del	GRCh38
NC_000006.11:g.35782592_35782604del , CM000668.1:g.35782592_35782604del	GRCh37
NC_000006.10:g.35890570_35890582del	NCBI36
NG_012184.1:g.14522_14534del
NG_012184.2:g.14522_14534del
NG_012184.3:g.22610_22622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.649+33_649+45del MANE Select	ENSP00000353346.1:n.649+33_649+45del
ENST00000496656.2:n.428+33_428+45del
ENST00000651132.1:c.649+33_649+45del	ENSP00000498322.1:n.649+33_649+45del
ENST00000651676.1:c.649+33_649+45del	ENSP00000498699.1:n.649+33_649+45del
ENST00000651994.1:c.*70-4622_*70-4610del	ENSP00000498310.1:n.*70-4622_*70-4610del
ENST00000652718.1:c.481+33_481+45del	ENSP00000498866.1:n.481+33_481+45del
ENST00000360215.2:c.649+33_649+45del	ENSP00000353346.1:n.649+33_649+45del
ENST00000496656.1:n.428+33_428+45del
NM_182548.3:c.649+33_649+45del	NP_872354.1:n.649+33_649+45del
XM_011514403.1:c.649+33_649+45del	XP_011512705.1:n.649+33_649+45del
NM_182548.4:c.649+33_649+45del MANE Select	NP_872354.1:n.649+33_649+45del