Canonical Allele Identifier: CA650705107

Gene: LHFPL5

Linked Data

• COSMIC: COSN23968293

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35823477_35823478insT , CM000668.2:g.35823477_35823478insT	GRCh38
NC_000006.11:g.35791254_35791255insT , CM000668.1:g.35791254_35791255insT	GRCh37
NC_000006.10:g.35899232_35899233insT	NCBI36
NG_012184.1:g.23184_23185insT
NG_012184.2:g.23184_23185insT
NG_012184.3:g.31272_31273insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.*512_*513insT MANE Select	ENSP00000353346.1:n.*512_*513insT
ENST00000496656.2:n.578+3657_578+3658insT
ENST00000651132.1:c.*512_*513insT	ENSP00000498322.1:n.*512_*513insT
ENST00000651676.1:c.*16+4014_*16+4015insT	ENSP00000498699.1:n.*16+4014_*16+4015insT
ENST00000651994.1:c.*592_*593insT	ENSP00000498310.1:n.*592_*593insT
ENST00000652718.1:c.508+4014_508+4015insT	ENSP00000498866.1:n.508+4014_508+4015insT
ENST00000360215.2:c.*512_*513insT	ENSP00000353346.1:n.*512_*513insT
ENST00000496656.1:n.812+3657_812+3658insT
NM_182548.3:c.*512_*513insT	NP_872354.1:n.*512_*513insT
NM_182548.4:c.*512_*513insT MANE Select	NP_872354.1:n.*512_*513insT