Canonical Allele Identifier: CA367870801

Gene: HGF

Linked Data

• dbSNP Id: rs2115927993
• MyVariant Identifiers: chr7:g.81358960G>A (hg19) ; chr7:g.81729644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729644G>A , CM000669.2:g.81729644G>A	GRCh38
NC_000007.13:g.81358960G>A , CM000669.1:g.81358960G>A	GRCh37
NC_000007.12:g.81196896G>A	NCBI36
NG_016274.1:g.45493C>T
NG_016274.2:g.45493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1001C>T MANE Select	ENSP00000222390.5:p.Pro334Leu
ENST00000457544.7:c.986C>T	ENSP00000391238.2:p.Pro329Leu
ENST00000222390.9:c.1001C>T	ENSP00000222390.5:p.Pro334Leu
ENST00000457544.6:c.986C>T	ENSP00000391238.2:p.Pro329Leu
NM_000601.4:c.1001C>T	NP_000592.3:p.Pro334Leu
NM_001010932.1:c.986C>T	NP_001010932.1:p.Pro329Leu
XM_006715956.2:c.1001C>T	XP_006716019.1:p.Pro334Leu
XM_011516115.1:c.986C>T	XP_011514417.1:p.Pro329Leu
NM_000601.5:c.1001C>T	NP_000592.3:p.Pro334Leu
NM_001010932.2:c.986C>T	NP_001010932.1:p.Pro329Leu
XM_011516115.2:c.986C>T	XP_011514417.1:p.Pro329Leu
NM_000601.6:c.1001C>T MANE Select	NP_000592.3:p.Pro334Leu
NM_001010932.3:c.986C>T	NP_001010932.1:p.Pro329Leu