Canonical Allele Identifier: CA1621068865

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1768920629
• gnomAD v4: 6-35823634-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823634_35823635insT , CM000668.2:g.35823634_35823635insT	GRCh38
NC_000006.11:g.35791411_35791412insT , CM000668.1:g.35791411_35791412insT	GRCh37
NC_000006.10:g.35899389_35899390insT	NCBI36
NG_012184.1:g.23341_23342insT
NG_012184.2:g.23341_23342insT
NG_012184.3:g.31429_31430insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*669_*670insT MANE Select	ENSP00000353346.1:n.*669_*670insT
ENST00000496656.2:n.578+3814_578+3815insT
ENST00000651132.1:c.*669_*670insT	ENSP00000498322.1:n.*669_*670insT
ENST00000651676.1:c.*16+4171_*16+4172insT	ENSP00000498699.1:n.*16+4171_*16+4172insT
ENST00000651994.1:c.*749_*750insT	ENSP00000498310.1:n.*749_*750insT
ENST00000652718.1:c.508+4171_508+4172insT	ENSP00000498866.1:n.508+4171_508+4172insT
ENST00000360215.2:c.*669_*670insT	ENSP00000353346.1:n.*669_*670insT
ENST00000496656.1:n.812+3814_812+3815insT
NM_182548.3:c.*669_*670insT	NP_872354.1:n.*669_*670insT
NM_182548.4:c.*669_*670insT MANE Select	NP_872354.1:n.*669_*670insT