Canonical Allele Identifier: CA2678434212

Gene: LHFPL5

Linked Data

• gnomAD v4: 6-35823731-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823737del , CM000668.2:g.35823737del	GRCh38
NC_000006.11:g.35791514del , CM000668.1:g.35791514del	GRCh37
NC_000006.10:g.35899492del	NCBI36
NG_012184.1:g.23444del
NG_012184.2:g.23444del
NG_012184.3:g.31532del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*772del MANE Select	ENSP00000353346.1:n.*772del
ENST00000496656.2:n.578+3917del
ENST00000651132.1:c.*772del	ENSP00000498322.1:n.*772del
ENST00000651676.1:c.*16+4274del	ENSP00000498699.1:n.*16+4274del
ENST00000651994.1:c.*852del	ENSP00000498310.1:n.*852del
ENST00000652718.1:c.508+4274del	ENSP00000498866.1:n.508+4274del
ENST00000360215.2:c.*772del	ENSP00000353346.1:n.*772del
ENST00000496656.1:n.812+3917del
NM_182548.3:c.*772del	NP_872354.1:n.*772del
NM_182548.4:c.*772del MANE Select	NP_872354.1:n.*772del