Canonical Allele Identifier: CA13344641

Gene: LHPP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124587345G>A , CM000672.2:g.124587345G>A	GRCh38
NC_000010.10:g.126275914G>A , CM000672.1:g.126275914G>A	GRCh37
NC_000010.9:g.126265904G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368842.10:c.717-25919G>A MANE Select	ENSP00000357835.5:n.717-25919G>A
ENST00000368839.1:c.625-25919G>A	ENSP00000357832.1:n.625-25919G>A
ENST00000368842.9:c.717-25919G>A	ENSP00000357835.5:n.717-25919G>A
ENST00000482963.1:n.166-25919G>A
ENST00000493240.1:n.207-25919G>A
NM_001167880.1:c.625-25919G>A	NP_001161352.1:n.625-25919G>A
NM_022126.3:c.717-25919G>A	NP_071409.3:n.717-25919G>A
XM_005270026.2:c.832-25919G>A	XP_005270083.1:n.832-25919G>A
XM_006717943.1:c.788+7532G>A	XP_006718006.1:n.788+7532G>A
XM_011540056.1:c.*19+23925G>A	XP_011538358.1:n.*19+23925G>A
XR_945797.1:n.835+23925G>A
NM_001318331.1:c.468-25919G>A	NP_001305260.1:n.468-25919G>A
XM_005270026.4:c.832-25919G>A	XP_005270083.1:n.832-25919G>A
NM_022126.4:c.717-25919G>A MANE Select	NP_071409.3:n.717-25919G>A
NM_001167880.2:c.625-25919G>A	NP_001161352.1:n.625-25919G>A
NM_001318331.2:c.468-25919G>A	NP_001305260.1:n.468-25919G>A