Canonical Allele Identifier: CA2678433169

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35814657-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814659del , CM000668.2:g.35814659del	GRCh38
NC_000006.11:g.35782436del , CM000668.1:g.35782436del	GRCh37
NC_000006.10:g.35890414del	NCBI36
NG_012184.1:g.14366del
NG_012184.2:g.14366del
NG_012184.3:g.22454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.526del MANE Select	ENSP00000353346.1:p.Arg176AlafsTer?
ENST00000496656.2:n.305del
ENST00000651132.1:c.526del	ENSP00000498322.1:p.Arg176AlafsTer?
ENST00000651676.1:c.526del	ENSP00000498699.1:p.Arg176AlafsTer?
ENST00000651994.1:c.*70-4778del	ENSP00000498310.1:n.*70-4778del
ENST00000652718.1:c.358del	ENSP00000498866.1:p.Arg120AlafsTer?
ENST00000360215.2:c.526del	ENSP00000353346.1:p.Arg176AlafsTer?
ENST00000496656.1:n.305del
NM_182548.3:c.526del	NP_872354.1:p.Arg176AlafsTer?
XM_011514403.1:c.526del	XP_011512705.1:p.Arg176AlafsTer?
NM_182548.4:c.526del MANE Select	NP_872354.1:p.Arg176AlafsTer?