Canonical Allele Identifier: CA2683530495

Gene: HGF

Linked Data

• gnomAD v4: 7-81711478-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711478T>C , CM000669.2:g.81711478T>C	GRCh38
NC_000007.13:g.81340794T>C , CM000669.1:g.81340794T>C	GRCh37
NC_000007.12:g.81178730T>C	NCBI36
NG_016274.1:g.63659A>G
NG_016274.2:g.63659A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1444+3A>G MANE Select	ENSP00000222390.5:n.1444+3A>G
ENST00000457544.7:c.1429+3A>G	ENSP00000391238.2:n.1429+3A>G
ENST00000222390.9:c.1444+3A>G	ENSP00000222390.5:n.1444+3A>G
ENST00000457544.6:c.1429+3A>G	ENSP00000391238.2:n.1429+3A>G
NM_000601.4:c.1444+3A>G	NP_000592.3:n.1444+3A>G
NM_001010932.1:c.1429+3A>G	NP_001010932.1:n.1429+3A>G
XM_006715956.2:c.1444+3A>G	XP_006716019.1:n.1444+3A>G
XM_011516115.1:c.1429+3A>G	XP_011514417.1:n.1429+3A>G
NM_000601.5:c.1444+3A>G	NP_000592.3:n.1444+3A>G
NM_001010932.2:c.1429+3A>G	NP_001010932.1:n.1429+3A>G
XM_011516115.2:c.1429+3A>G	XP_011514417.1:n.1429+3A>G
NM_000601.6:c.1444+3A>G MANE Select	NP_000592.3:n.1444+3A>G
NM_001010932.3:c.1429+3A>G	NP_001010932.1:n.1429+3A>G