Canonical Allele Identifier: CA2578923770

Gene: HGF

Linked Data

• gnomAD v4: 7-81711514-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711516del , CM000669.2:g.81711516del	GRCh38
NC_000007.13:g.81340832del , CM000669.1:g.81340832del	GRCh37
NC_000007.12:g.81178768del	NCBI36
NG_016274.1:g.63622del
NG_016274.2:g.63622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1410del MANE Select	ENSP00000222390.5:p.Gly471ValfsTer7
ENST00000457544.7:c.1395del	ENSP00000391238.2:p.Gly466ValfsTer7
ENST00000222390.9:c.1410del	ENSP00000222390.5:p.Gly471ValfsTer7
ENST00000457544.6:c.1395del	ENSP00000391238.2:p.Gly466ValfsTer7
NM_000601.4:c.1410del	NP_000592.3:p.Gly471ValfsTer7
NM_001010932.1:c.1395del	NP_001010932.1:p.Gly466ValfsTer7
XM_006715956.2:c.1410del	XP_006716019.1:p.Gly471ValfsTer7
XM_011516115.1:c.1395del	XP_011514417.1:p.Gly466ValfsTer7
NM_000601.5:c.1410del	NP_000592.3:p.Gly471ValfsTer7
NM_001010932.2:c.1395del	NP_001010932.1:p.Gly466ValfsTer7
XM_011516115.2:c.1395del	XP_011514417.1:p.Gly466ValfsTer7
NM_000601.6:c.1410del MANE Select	NP_000592.3:p.Gly471ValfsTer7
NM_001010932.3:c.1395del	NP_001010932.1:p.Gly466ValfsTer7