Canonical Allele Identifier: CA2578923841

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726038_81726040dup , CM000669.2:g.81726038_81726040dup	GRCh38
NC_000007.13:g.81355354_81355356dup , CM000669.1:g.81355354_81355356dup	GRCh37
NC_000007.12:g.81193290_81193292dup	NCBI36
NG_016274.1:g.49098_49100dup
NG_016274.2:g.49098_49100dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1041-22_1041-20dup MANE Select	ENSP00000222390.5:n.1041-22_1041-20dup
ENST00000457544.7:c.1026-22_1026-20dup	ENSP00000391238.2:n.1026-22_1026-20dup
ENST00000222390.9:c.1041-22_1041-20dup	ENSP00000222390.5:n.1041-22_1041-20dup
ENST00000457544.6:c.1026-22_1026-20dup	ENSP00000391238.2:n.1026-22_1026-20dup
NM_000601.4:c.1041-22_1041-20dup	NP_000592.3:n.1041-22_1041-20dup
NM_001010932.1:c.1026-22_1026-20dup	NP_001010932.1:n.1026-22_1026-20dup
XM_006715956.2:c.1041-22_1041-20dup	XP_006716019.1:n.1041-22_1041-20dup
XM_011516115.1:c.1026-22_1026-20dup	XP_011514417.1:n.1026-22_1026-20dup
NM_000601.5:c.1041-22_1041-20dup	NP_000592.3:n.1041-22_1041-20dup
NM_001010932.2:c.1026-22_1026-20dup	NP_001010932.1:n.1026-22_1026-20dup
XM_011516115.2:c.1026-22_1026-20dup	XP_011514417.1:n.1026-22_1026-20dup
NM_000601.6:c.1041-22_1041-20dup MANE Select	NP_000592.3:n.1041-22_1041-20dup
NM_001010932.3:c.1026-22_1026-20dup	NP_001010932.1:n.1026-22_1026-20dup