Canonical Allele Identifier: CA456129170

Gene: HGF

Linked Data

• gnomAD v4: 7-81729688-G-T
• MyVariant Identifiers: chr7:g.81359004G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729688G>T , CM000669.2:g.81729688G>T	GRCh38
NC_000007.13:g.81359004G>T , CM000669.1:g.81359004G>T	GRCh37
NC_000007.12:g.81196940G>T	NCBI36
NG_016274.1:g.45449C>A
NG_016274.2:g.45449C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.957C>A MANE Select	ENSP00000222390.5:p.Thr319=
ENST00000457544.7:c.942C>A	ENSP00000391238.2:p.Thr314=
ENST00000222390.9:c.957C>A	ENSP00000222390.5:p.Thr319=
ENST00000457544.6:c.942C>A	ENSP00000391238.2:p.Thr314=
NM_000601.4:c.957C>A	NP_000592.3:p.Thr319=
NM_001010932.1:c.942C>A	NP_001010932.1:p.Thr314=
XM_006715956.2:c.957C>A	XP_006716019.1:p.Thr319=
XM_011516115.1:c.942C>A	XP_011514417.1:p.Thr314=
NM_000601.5:c.957C>A	NP_000592.3:p.Thr319=
NM_001010932.2:c.942C>A	NP_001010932.1:p.Thr314=
XM_011516115.2:c.942C>A	XP_011514417.1:p.Thr314=
NM_000601.6:c.957C>A MANE Select	NP_000592.3:p.Thr319=
NM_001010932.3:c.942C>A	NP_001010932.1:p.Thr314=