Canonical Allele Identifier: CA824259693

Gene: LHFPL5

Linked Data

• dbSNP Id: rs1341062494
• MyVariant Identifiers: chr6:g.35791301_35791302insGG (hg19) ; chr6:g.35823524_35823525insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823526_35823527dup , CM000668.2:g.35823526_35823527dup	GRCh38
NC_000006.11:g.35791303_35791304dup , CM000668.1:g.35791303_35791304dup	GRCh37
NC_000006.10:g.35899281_35899282dup	NCBI36
NG_012184.1:g.23233_23234dup
NG_012184.2:g.23233_23234dup
NG_012184.3:g.31321_31322dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360215.3:c.*561_*562dup MANE Select	ENSP00000353346.1:n.*561_*562dup
ENST00000496656.2:n.578+3706_578+3707dup
ENST00000651132.1:c.*561_*562dup	ENSP00000498322.1:n.*561_*562dup
ENST00000651676.1:c.*16+4063_*16+4064dup	ENSP00000498699.1:n.*16+4063_*16+4064dup
ENST00000651994.1:c.*641_*642dup	ENSP00000498310.1:n.*641_*642dup
ENST00000652718.1:c.508+4063_508+4064dup	ENSP00000498866.1:n.508+4063_508+4064dup
ENST00000360215.2:c.*561_*562dup	ENSP00000353346.1:n.*561_*562dup
ENST00000496656.1:n.812+3706_812+3707dup
NM_182548.3:c.*561_*562dup	NP_872354.1:n.*561_*562dup
NM_182548.4:c.*561_*562dup MANE Select	NP_872354.1:n.*561_*562dup