Canonical Allele Identifier: CA2683531111

Gene: HGF

Linked Data

• gnomAD v4: 7-81726138-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726138G>C , CM000669.2:g.81726138G>C	GRCh38
NC_000007.13:g.81355454G>C , CM000669.1:g.81355454G>C	GRCh37
NC_000007.12:g.81193390G>C	NCBI36
NG_016274.1:g.48999C>G
NG_016274.2:g.48999C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1041-121C>G MANE Select	ENSP00000222390.5:n.1041-121C>G
ENST00000457544.7:c.1026-121C>G	ENSP00000391238.2:n.1026-121C>G
ENST00000222390.9:c.1041-121C>G	ENSP00000222390.5:n.1041-121C>G
ENST00000457544.6:c.1026-121C>G	ENSP00000391238.2:n.1026-121C>G
NM_000601.4:c.1041-121C>G	NP_000592.3:n.1041-121C>G
NM_001010932.1:c.1026-121C>G	NP_001010932.1:n.1026-121C>G
XM_006715956.2:c.1041-121C>G	XP_006716019.1:n.1041-121C>G
XM_011516115.1:c.1026-121C>G	XP_011514417.1:n.1026-121C>G
NM_000601.5:c.1041-121C>G	NP_000592.3:n.1041-121C>G
NM_001010932.2:c.1026-121C>G	NP_001010932.1:n.1026-121C>G
XM_011516115.2:c.1026-121C>G	XP_011514417.1:n.1026-121C>G
NM_000601.6:c.1041-121C>G MANE Select	NP_000592.3:n.1041-121C>G
NM_001010932.3:c.1026-121C>G	NP_001010932.1:n.1026-121C>G