Canonical Allele Identifier: CA367873439

Gene: HGF

Linked Data

• gnomAD v4: 7-81711495-A-G
• MyVariant Identifiers: chr7:g.81340811A>G (hg19) ; chr7:g.81711495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81711495A>G , CM000669.2:g.81711495A>G	GRCh38
NC_000007.13:g.81340811A>G , CM000669.1:g.81340811A>G	GRCh37
NC_000007.12:g.81178747A>G	NCBI36
NG_016274.1:g.63642T>C
NG_016274.2:g.63642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1430T>C MANE Select	ENSP00000222390.5:p.Ile477Thr
ENST00000457544.7:c.1415T>C	ENSP00000391238.2:p.Ile472Thr
ENST00000222390.9:c.1430T>C	ENSP00000222390.5:p.Ile477Thr
ENST00000457544.6:c.1415T>C	ENSP00000391238.2:p.Ile472Thr
NM_000601.4:c.1430T>C	NP_000592.3:p.Ile477Thr
NM_001010932.1:c.1415T>C	NP_001010932.1:p.Ile472Thr
XM_006715956.2:c.1430T>C	XP_006716019.1:p.Ile477Thr
XM_011516115.1:c.1415T>C	XP_011514417.1:p.Ile472Thr
NM_000601.5:c.1430T>C	NP_000592.3:p.Ile477Thr
NM_001010932.2:c.1415T>C	NP_001010932.1:p.Ile472Thr
XM_011516115.2:c.1415T>C	XP_011514417.1:p.Ile472Thr
NM_000601.6:c.1430T>C MANE Select	NP_000592.3:p.Ile477Thr
NM_001010932.3:c.1415T>C	NP_001010932.1:p.Ile472Thr