Canonical Allele Identifier: CA1720883868

Gene: HGF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81726192_81726193delinsCA , CM000669.2:g.81726192_81726193delinsCA	GRCh38
NC_000007.13:g.81355508_81355509delinsCA , CM000669.1:g.81355508_81355509delinsCA	GRCh37
NC_000007.12:g.81193444_81193445delinsCA	NCBI36
NG_016274.1:g.48944_48945delinsTG
NG_016274.2:g.48944_48945delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222390.11:c.1041-176_1041-175delinsTG MANE Select	ENSP00000222390.5:n.1041-176_1041-175delinsTG
ENST00000457544.7:c.1026-176_1026-175delinsTG	ENSP00000391238.2:n.1026-176_1026-175delinsTG
ENST00000222390.9:c.1041-176_1041-175delinsTG	ENSP00000222390.5:n.1041-176_1041-175delinsTG
ENST00000457544.6:c.1026-176_1026-175delinsTG	ENSP00000391238.2:n.1026-176_1026-175delinsTG
NM_000601.4:c.1041-176_1041-175delinsTG	NP_000592.3:n.1041-176_1041-175delinsTG
NM_001010932.1:c.1026-176_1026-175delinsTG	NP_001010932.1:n.1026-176_1026-175delinsTG
XM_006715956.2:c.1041-176_1041-175delinsTG	XP_006716019.1:n.1041-176_1041-175delinsTG
XM_011516115.1:c.1026-176_1026-175delinsTG	XP_011514417.1:n.1026-176_1026-175delinsTG
NM_000601.5:c.1041-176_1041-175delinsTG	NP_000592.3:n.1041-176_1041-175delinsTG
NM_001010932.2:c.1026-176_1026-175delinsTG	NP_001010932.1:n.1026-176_1026-175delinsTG
XM_011516115.2:c.1026-176_1026-175delinsTG	XP_011514417.1:n.1026-176_1026-175delinsTG
NM_000601.6:c.1041-176_1041-175delinsTG MANE Select	NP_000592.3:n.1041-176_1041-175delinsTG
NM_001010932.3:c.1026-176_1026-175delinsTG	NP_001010932.1:n.1026-176_1026-175delinsTG