Canonical Allele Identifier: CA1720890529

Gene: HGF

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81734871C>G , CM000669.2:g.81734871C>G	GRCh38
NC_000007.13:g.81364187C>G , CM000669.1:g.81364187C>G	GRCh37
NC_000007.12:g.81202123C>G	NCBI36
NG_016274.1:g.40266G>C
NG_016274.2:g.40266G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.866-5092G>C MANE Select	ENSP00000222390.5:n.866-5092G>C
ENST00000457544.7:c.851-5092G>C	ENSP00000391238.2:n.851-5092G>C
ENST00000222390.9:c.866-5092G>C	ENSP00000222390.5:n.866-5092G>C
ENST00000457544.6:c.851-5092G>C	ENSP00000391238.2:n.851-5092G>C
NM_000601.4:c.866-5092G>C	NP_000592.3:n.866-5092G>C
NM_001010932.1:c.851-5092G>C	NP_001010932.1:n.851-5092G>C
XM_006715956.2:c.866-5092G>C	XP_006716019.1:n.866-5092G>C
XM_011516115.1:c.851-5092G>C	XP_011514417.1:n.851-5092G>C
NM_000601.5:c.866-5092G>C	NP_000592.3:n.866-5092G>C
NM_001010932.2:c.851-5092G>C	NP_001010932.1:n.851-5092G>C
XM_011516115.2:c.851-5092G>C	XP_011514417.1:n.851-5092G>C
NM_000601.6:c.866-5092G>C MANE Select	NP_000592.3:n.866-5092G>C
NM_001010932.3:c.851-5092G>C	NP_001010932.1:n.851-5092G>C