Canonical Allele Identifier: CA2683531114

Gene: HGF

Linked Data

• gnomAD v4: 7-81726140-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726140A>G , CM000669.2:g.81726140A>G	GRCh38
NC_000007.13:g.81355456A>G , CM000669.1:g.81355456A>G	GRCh37
NC_000007.12:g.81193392A>G	NCBI36
NG_016274.1:g.48997T>C
NG_016274.2:g.48997T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1041-123T>C MANE Select	ENSP00000222390.5:n.1041-123T>C
ENST00000457544.7:c.1026-123T>C	ENSP00000391238.2:n.1026-123T>C
ENST00000222390.9:c.1041-123T>C	ENSP00000222390.5:n.1041-123T>C
ENST00000457544.6:c.1026-123T>C	ENSP00000391238.2:n.1026-123T>C
NM_000601.4:c.1041-123T>C	NP_000592.3:n.1041-123T>C
NM_001010932.1:c.1026-123T>C	NP_001010932.1:n.1026-123T>C
XM_006715956.2:c.1041-123T>C	XP_006716019.1:n.1041-123T>C
XM_011516115.1:c.1026-123T>C	XP_011514417.1:n.1026-123T>C
NM_000601.5:c.1041-123T>C	NP_000592.3:n.1041-123T>C
NM_001010932.2:c.1026-123T>C	NP_001010932.1:n.1026-123T>C
XM_011516115.2:c.1026-123T>C	XP_011514417.1:n.1026-123T>C
NM_000601.6:c.1041-123T>C MANE Select	NP_000592.3:n.1041-123T>C
NM_001010932.3:c.1026-123T>C	NP_001010932.1:n.1026-123T>C