Canonical Allele Identifier: CA367870781

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81358951T>A (hg19) ; chr7:g.81729635T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729635T>A , CM000669.2:g.81729635T>A	GRCh38
NC_000007.13:g.81358951T>A , CM000669.1:g.81358951T>A	GRCh37
NC_000007.12:g.81196887T>A	NCBI36
NG_016274.1:g.45502A>T
NG_016274.2:g.45502A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1010A>T MANE Select	ENSP00000222390.5:p.His337Leu
ENST00000457544.7:c.995A>T	ENSP00000391238.2:p.His332Leu
ENST00000222390.9:c.1010A>T	ENSP00000222390.5:p.His337Leu
ENST00000457544.6:c.995A>T	ENSP00000391238.2:p.His332Leu
NM_000601.4:c.1010A>T	NP_000592.3:p.His337Leu
NM_001010932.1:c.995A>T	NP_001010932.1:p.His332Leu
XM_006715956.2:c.1010A>T	XP_006716019.1:p.His337Leu
XM_011516115.1:c.995A>T	XP_011514417.1:p.His332Leu
NM_000601.5:c.1010A>T	NP_000592.3:p.His337Leu
NM_001010932.2:c.995A>T	NP_001010932.1:p.His332Leu
XM_011516115.2:c.995A>T	XP_011514417.1:p.His332Leu
NM_000601.6:c.1010A>T MANE Select	NP_000592.3:p.His337Leu
NM_001010932.3:c.995A>T	NP_001010932.1:p.His332Leu