Canonical Allele Identifier: CA164388080

Gene: LHFPL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.104863366G>A , CM000669.2:g.104863366G>A	GRCh38
NC_000007.13:g.104503813G>A , CM000669.1:g.104503813G>A	GRCh37
NC_000007.12:g.104291049G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401970.3:c.*31+17937G>A	ENSP00000385374.3:n.*31+17937G>A
ENST00000424859.7:c.683-42821G>A MANE Select	ENSP00000393128.2:n.683-42821G>A
ENST00000683240.1:c.673-42821G>A
ENST00000684090.1:n.261-42821G>A
ENST00000424859.6:c.641-42821G>A	ENSP00000393128.1:n.641-42821G>A
ENST00000401970.2:c.*31+17937G>A	ENSP00000385374.2:n.*31+17937G>A
ENST00000424859.5:c.641-42821G>A	ENSP00000393128.1:n.641-42821G>A
NM_199000.2:c.683-42821G>A	NP_945351.1:n.683-42821G>A
XM_005250327.1:c.*31+17937G>A	XP_005250384.1:n.*31+17937G>A
XM_005250327.2:c.*31+17937G>A	XP_005250384.1:n.*31+17937G>A
NM_001386065.1:c.*31+17937G>A	NP_001372994.1:n.*31+17937G>A
NM_199000.3:c.683-42821G>A MANE Select	NP_945351.1:n.683-42821G>A