Canonical Allele Identifier: CA367874098

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81717363T>A , CM000669.2:g.81717363T>A	GRCh38
NC_000007.13:g.81346679T>A , CM000669.1:g.81346679T>A	GRCh37
NC_000007.12:g.81184615T>A	NCBI36
NG_016274.1:g.57774A>T
NG_016274.2:g.57774A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000601.6:c.1274A>T MANE Select	NP_000592.3:p.His425Leu
ENST00000222390.11:c.1274A>T MANE Select	ENSP00000222390.5:p.His425Leu
NM_000601.4:c.1274A>T	NP_000592.3:p.His425Leu
NM_000601.5:c.1274A>T	NP_000592.3:p.His425Leu
NM_001010932.1:c.1259A>T	NP_001010932.1:p.His420Leu
NM_001010932.2:c.1259A>T	NP_001010932.1:p.His420Leu
NM_001010932.3:c.1259A>T	NP_001010932.1:p.His420Leu
ENST00000222390.9:c.1274A>T	ENSP00000222390.5:p.His425Leu
ENST00000457544.6:c.1259A>T	ENSP00000391238.2:p.His420Leu
ENST00000457544.7:c.1259A>T	ENSP00000391238.2:p.His420Leu
XM_006715956.2:c.1274A>T	XP_006716019.1:p.His425Leu
XM_011516115.1:c.1259A>T	XP_011514417.1:p.His420Leu
XM_011516115.2:c.1259A>T	XP_011514417.1:p.His420Leu