Canonical Allele Identifier: CA367870773

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81358948T>A (hg19) ; chr7:g.81729632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729632T>A , CM000669.2:g.81729632T>A	GRCh38
NC_000007.13:g.81358948T>A , CM000669.1:g.81358948T>A	GRCh37
NC_000007.12:g.81196884T>A	NCBI36
NG_016274.1:g.45505A>T
NG_016274.2:g.45505A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1013A>T MANE Select	ENSP00000222390.5:p.Asp338Val
ENST00000457544.7:c.998A>T	ENSP00000391238.2:p.Asp333Val
ENST00000222390.9:c.1013A>T	ENSP00000222390.5:p.Asp338Val
ENST00000457544.6:c.998A>T	ENSP00000391238.2:p.Asp333Val
NM_000601.4:c.1013A>T	NP_000592.3:p.Asp338Val
NM_001010932.1:c.998A>T	NP_001010932.1:p.Asp333Val
XM_006715956.2:c.1013A>T	XP_006716019.1:p.Asp338Val
XM_011516115.1:c.998A>T	XP_011514417.1:p.Asp333Val
NM_000601.5:c.1013A>T	NP_000592.3:p.Asp338Val
NM_001010932.2:c.998A>T	NP_001010932.1:p.Asp333Val
XM_011516115.2:c.998A>T	XP_011514417.1:p.Asp333Val
NM_000601.6:c.1013A>T MANE Select	NP_000592.3:p.Asp338Val
NM_001010932.3:c.998A>T	NP_001010932.1:p.Asp333Val