Canonical Allele Identifier: CA2683531047

Gene: HGF

Linked Data

• gnomAD v4: 7-81725952-TCAGTGGTAAAACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725954_81725966del , CM000669.2:g.81725954_81725966del	GRCh38
NC_000007.13:g.81355270_81355282del , CM000669.1:g.81355270_81355282del	GRCh37
NC_000007.12:g.81193206_81193218del	NCBI36
NG_016274.1:g.49172_49184del
NG_016274.2:g.49172_49184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1093_1105del MANE Select	ENSP00000222390.5:p.Cys365IlefsTer?
ENST00000457544.7:c.1078_1090del	ENSP00000391238.2:p.Cys360IlefsTer?
ENST00000222390.9:c.1093_1105del	ENSP00000222390.5:p.Cys365IlefsTer?
ENST00000457544.6:c.1078_1090del	ENSP00000391238.2:p.Cys360IlefsTer?
NM_000601.4:c.1093_1105del	NP_000592.3:p.Cys365IlefsTer?
NM_001010932.1:c.1078_1090del	NP_001010932.1:p.Cys360IlefsTer?
XM_006715956.2:c.1093_1105del	XP_006716019.1:p.Cys365IlefsTer?
XM_011516115.1:c.1078_1090del	XP_011514417.1:p.Cys360IlefsTer?
NM_000601.5:c.1093_1105del	NP_000592.3:p.Cys365IlefsTer?
NM_001010932.2:c.1078_1090del	NP_001010932.1:p.Cys360IlefsTer?
XM_011516115.2:c.1078_1090del	XP_011514417.1:p.Cys360IlefsTer?
NM_000601.6:c.1093_1105del MANE Select	NP_000592.3:p.Cys365IlefsTer?
NM_001010932.3:c.1078_1090del	NP_001010932.1:p.Cys360IlefsTer?