Canonical Allele Identifier: CA456129009

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81355261G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81725945G>A , CM000669.2:g.81725945G>A	GRCh38
NC_000007.13:g.81355261G>A , CM000669.1:g.81355261G>A	GRCh37
NC_000007.12:g.81193197G>A	NCBI36
NG_016274.1:g.49192C>T
NG_016274.2:g.49192C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1113C>T MANE Select	ENSP00000222390.5:p.Asn371=
ENST00000457544.7:c.1098C>T	ENSP00000391238.2:p.Asn366=
ENST00000222390.9:c.1113C>T	ENSP00000222390.5:p.Asn371=
ENST00000457544.6:c.1098C>T	ENSP00000391238.2:p.Asn366=
NM_000601.4:c.1113C>T	NP_000592.3:p.Asn371=
NM_001010932.1:c.1098C>T	NP_001010932.1:p.Asn366=
XM_006715956.2:c.1113C>T	XP_006716019.1:p.Asn371=
XM_011516115.1:c.1098C>T	XP_011514417.1:p.Asn366=
NM_000601.5:c.1113C>T	NP_000592.3:p.Asn371=
NM_001010932.2:c.1098C>T	NP_001010932.1:p.Asn366=
XM_011516115.2:c.1098C>T	XP_011514417.1:p.Asn366=
NM_000601.6:c.1113C>T MANE Select	NP_000592.3:p.Asn371=
NM_001010932.3:c.1098C>T	NP_001010932.1:p.Asn366=