Canonical Allele Identifier: CA650705099

Gene: LHFPL5

Linked Data

• COSMIC: COSN20426229 ; COSN23812474

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823422_35823423insT , CM000668.2:g.35823422_35823423insT	GRCh38
NC_000006.11:g.35791199_35791200insT , CM000668.1:g.35791199_35791200insT	GRCh37
NC_000006.10:g.35899177_35899178insT	NCBI36
NG_012184.1:g.23129_23130insT
NG_012184.2:g.23129_23130insT
NG_012184.3:g.31217_31218insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*457_*458insT MANE Select	ENSP00000353346.1:n.*457_*458insT
ENST00000496656.2:n.578+3602_578+3603insT
ENST00000651132.1:c.*457_*458insT	ENSP00000498322.1:n.*457_*458insT
ENST00000651676.1:c.*16+3959_*16+3960insT	ENSP00000498699.1:n.*16+3959_*16+3960insT
ENST00000651994.1:c.*537_*538insT	ENSP00000498310.1:n.*537_*538insT
ENST00000652718.1:c.508+3959_508+3960insT	ENSP00000498866.1:n.508+3959_508+3960insT
ENST00000360215.2:c.*457_*458insT	ENSP00000353346.1:n.*457_*458insT
ENST00000496656.1:n.812+3602_812+3603insT
NM_182548.3:c.*457_*458insT	NP_872354.1:n.*457_*458insT
NM_182548.4:c.*457_*458insT MANE Select	NP_872354.1:n.*457_*458insT