Canonical Allele Identifier: CA2683531107

Gene: HGF

Linked Data

• gnomAD v4: 7-81726134-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726134T>G , CM000669.2:g.81726134T>G	GRCh38
NC_000007.13:g.81355450T>G , CM000669.1:g.81355450T>G	GRCh37
NC_000007.12:g.81193386T>G	NCBI36
NG_016274.1:g.49003A>C
NG_016274.2:g.49003A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1041-117A>C MANE Select	ENSP00000222390.5:n.1041-117A>C
ENST00000457544.7:c.1026-117A>C	ENSP00000391238.2:n.1026-117A>C
ENST00000222390.9:c.1041-117A>C	ENSP00000222390.5:n.1041-117A>C
ENST00000457544.6:c.1026-117A>C	ENSP00000391238.2:n.1026-117A>C
NM_000601.4:c.1041-117A>C	NP_000592.3:n.1041-117A>C
NM_001010932.1:c.1026-117A>C	NP_001010932.1:n.1026-117A>C
XM_006715956.2:c.1041-117A>C	XP_006716019.1:n.1041-117A>C
XM_011516115.1:c.1026-117A>C	XP_011514417.1:n.1026-117A>C
NM_000601.5:c.1041-117A>C	NP_000592.3:n.1041-117A>C
NM_001010932.2:c.1026-117A>C	NP_001010932.1:n.1026-117A>C
XM_011516115.2:c.1026-117A>C	XP_011514417.1:n.1026-117A>C
NM_000601.6:c.1041-117A>C MANE Select	NP_000592.3:n.1041-117A>C
NM_001010932.3:c.1026-117A>C	NP_001010932.1:n.1026-117A>C