Canonical Allele Identifier: CA367869954

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81355254C>T (hg19) ; chr7:g.81725938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725938C>T , CM000669.2:g.81725938C>T	GRCh38
NC_000007.13:g.81355254C>T , CM000669.1:g.81355254C>T	GRCh37
NC_000007.12:g.81193190C>T	NCBI36
NG_016274.1:g.49199G>A
NG_016274.2:g.49199G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1120G>A MANE Select	ENSP00000222390.5:p.Val374Ile
ENST00000457544.7:c.1105G>A	ENSP00000391238.2:p.Val369Ile
ENST00000222390.9:c.1120G>A	ENSP00000222390.5:p.Val374Ile
ENST00000457544.6:c.1105G>A	ENSP00000391238.2:p.Val369Ile
NM_000601.4:c.1120G>A	NP_000592.3:p.Val374Ile
NM_001010932.1:c.1105G>A	NP_001010932.1:p.Val369Ile
XM_006715956.2:c.1120G>A	XP_006716019.1:p.Val374Ile
XM_011516115.1:c.1105G>A	XP_011514417.1:p.Val369Ile
NM_000601.5:c.1120G>A	NP_000592.3:p.Val374Ile
NM_001010932.2:c.1105G>A	NP_001010932.1:p.Val369Ile
XM_011516115.2:c.1105G>A	XP_011514417.1:p.Val369Ile
NM_000601.6:c.1120G>A MANE Select	NP_000592.3:p.Val374Ile
NM_001010932.3:c.1105G>A	NP_001010932.1:p.Val369Ile