Canonical Allele Identifier: CA842847950

Gene: HGF

Linked Data

• dbSNP Id: rs1301213883
• gnomAD v3: 7-81726185-CT-C
• gnomAD v4: 7-81726185-CT-C
• MyVariant Identifiers: chr7:g.81355502del (hg19) ; chr7:g.81726186del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726186del , CM000669.2:g.81726186del	GRCh38
NC_000007.13:g.81355502del , CM000669.1:g.81355502del	GRCh37
NC_000007.12:g.81193438del	NCBI36
NG_016274.1:g.48951del
NG_016274.2:g.48951del

Transcript Alleles

HGVS	Amino-acid change
ENST00000222390.11:c.1041-169del MANE Select	ENSP00000222390.5:n.1041-169del
ENST00000457544.7:c.1026-169del	ENSP00000391238.2:n.1026-169del
ENST00000222390.9:c.1041-169del	ENSP00000222390.5:n.1041-169del
ENST00000457544.6:c.1026-169del	ENSP00000391238.2:n.1026-169del
NM_000601.4:c.1041-169del	NP_000592.3:n.1041-169del
NM_001010932.1:c.1026-169del	NP_001010932.1:n.1026-169del
XM_006715956.2:c.1041-169del	XP_006716019.1:n.1041-169del
XM_011516115.1:c.1026-169del	XP_011514417.1:n.1026-169del
NM_000601.5:c.1041-169del	NP_000592.3:n.1041-169del
NM_001010932.2:c.1026-169del	NP_001010932.1:n.1026-169del
XM_011516115.2:c.1026-169del	XP_011514417.1:n.1026-169del
NM_000601.6:c.1041-169del MANE Select	NP_000592.3:n.1041-169del
NM_001010932.3:c.1026-169del	NP_001010932.1:n.1026-169del