Canonical Allele Identifier: CA4316822

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81706340G>A , CM000669.2:g.81706340G>A	GRCh38
NC_000007.13:g.81335656G>A , CM000669.1:g.81335656G>A	GRCh37
NC_000007.12:g.81173592G>A	NCBI36
NG_016274.1:g.68797C>T
NG_016274.2:g.68797C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000601.6:c.1704C>T MANE Select	NP_000592.3:p.Ser568=
ENST00000222390.11:c.1704C>T MANE Select	ENSP00000222390.5:p.Ser568=
NM_000601.4:c.1704C>T	NP_000592.3:p.Ser568=
NM_000601.5:c.1704C>T	NP_000592.3:p.Ser568=
NM_001010932.1:c.1689C>T	NP_001010932.1:p.Ser563=
NM_001010932.2:c.1689C>T	NP_001010932.1:p.Ser563=
NM_001010932.3:c.1689C>T	NP_001010932.1:p.Ser563=
ENST00000222390.9:c.1704C>T	ENSP00000222390.5:p.Ser568=
ENST00000457544.6:c.1689C>T	ENSP00000391238.2:p.Ser563=
ENST00000457544.7:c.1689C>T	ENSP00000391238.2:p.Ser563=
XM_006715956.2:c.1704C>T	XP_006716019.1:p.Ser568=
XM_011516115.1:c.1689C>T	XP_011514417.1:p.Ser563=
XM_011516115.2:c.1689C>T	XP_011514417.1:p.Ser563=