Canonical Allele Identifier: CA2683531199

Gene: HGF

Linked Data

• gnomAD v4: 7-81729582-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729584del , CM000669.2:g.81729584del	GRCh38
NC_000007.13:g.81358900del , CM000669.1:g.81358900del	GRCh37
NC_000007.12:g.81196836del	NCBI36
NG_016274.1:g.45554del
NG_016274.2:g.45554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1040+22del MANE Select	ENSP00000222390.5:n.1040+22del
ENST00000457544.7:c.1025+22del	ENSP00000391238.2:n.1025+22del
ENST00000222390.9:c.1040+22del	ENSP00000222390.5:n.1040+22del
ENST00000457544.6:c.1025+22del	ENSP00000391238.2:n.1025+22del
NM_000601.4:c.1040+22del	NP_000592.3:n.1040+22del
NM_001010932.1:c.1025+22del	NP_001010932.1:n.1025+22del
XM_006715956.2:c.1040+22del	XP_006716019.1:n.1040+22del
XM_011516115.1:c.1025+22del	XP_011514417.1:n.1025+22del
NM_000601.5:c.1040+22del	NP_000592.3:n.1040+22del
NM_001010932.2:c.1025+22del	NP_001010932.1:n.1025+22del
XM_011516115.2:c.1025+22del	XP_011514417.1:n.1025+22del
NM_000601.6:c.1040+22del MANE Select	NP_000592.3:n.1040+22del
NM_001010932.3:c.1025+22del	NP_001010932.1:n.1025+22del