Canonical Allele Identifier: CA2770639326

Gene: LHFPL5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35814808_35814814del , CM000668.2:g.35814808_35814814del	GRCh38
NC_000006.11:g.35782585_35782591del , CM000668.1:g.35782585_35782591del	GRCh37
NC_000006.10:g.35890563_35890569del	NCBI36
NG_012184.1:g.14515_14521del
NG_012184.2:g.14515_14521del
NG_012184.3:g.22603_22609del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360215.3:c.649+26_649+32del MANE Select	ENSP00000353346.1:n.649+26_649+32del
ENST00000496656.2:n.428+26_428+32del
ENST00000651132.1:c.649+26_649+32del	ENSP00000498322.1:n.649+26_649+32del
ENST00000651676.1:c.649+26_649+32del	ENSP00000498699.1:n.649+26_649+32del
ENST00000651994.1:c.*70-4629_*70-4623del	ENSP00000498310.1:n.*70-4629_*70-4623del
ENST00000652718.1:c.481+26_481+32del	ENSP00000498866.1:n.481+26_481+32del
ENST00000360215.2:c.649+26_649+32del	ENSP00000353346.1:n.649+26_649+32del
ENST00000496656.1:n.428+26_428+32del
NM_182548.3:c.649+26_649+32del	NP_872354.1:n.649+26_649+32del
XM_011514403.1:c.649+26_649+32del	XP_011512705.1:n.649+26_649+32del
NM_182548.4:c.649+26_649+32del MANE Select	NP_872354.1:n.649+26_649+32del