Canonical Allele Identifier: CA367870697

Gene: HGF

Linked Data

• MyVariant Identifiers: chr7:g.81358919A>C (hg19) ; chr7:g.81729603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.81729603A>C , CM000669.2:g.81729603A>C	GRCh38
NC_000007.13:g.81358919A>C , CM000669.1:g.81358919A>C	GRCh37
NC_000007.12:g.81196855A>C	NCBI36
NG_016274.1:g.45534T>G
NG_016274.2:g.45534T>G

Transcript Alleles

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