Canonical Allele Identifier: CA4448773

Gene: MET

Linked Data

• ClinVar Variation Id: 1932717
• ClinVar RCV Id: RCV002649494
• dbSNP Id: rs745810421
• ExAC: 7:116423534 G / A
• gnomAD v2: 7-116423534-G-A
• MyVariant Identifiers: chr7:g.116423534G>A (hg19) ; chr7:g.116783480G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783480G>A , CM000669.2:g.116783480G>A	GRCh38
NC_000007.13:g.116423534G>A , CM000669.1:g.116423534G>A	GRCh37
NC_000007.12:g.116210770G>A	NCBI36
NG_008996.1:g.116076G>A , LRG_662:g.116076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1403+11G>A	ENSP00000410980.2:n.*1403+11G>A
ENST00000318493.11:c.3852+11G>A	ENSP00000317272.6:n.3852+11G>A
ENST00000397752.8:c.3798+11G>A MANE Select	ENSP00000380860.3:n.3798+11G>A
ENST00000318493.10:c.3852+11G>A	ENSP00000317272.6:n.3852+11G>A
ENST00000397752.7:c.3798+11G>A	ENSP00000380860.3:n.3798+11G>A
NM_000245.2:c.3798+11G>A	NP_000236.2:n.3798+11G>A
NM_001127500.1:c.3852+11G>A , LRG_662t1:c.3852+11G>A	NP_001120972.1:n.3852+11G>A
XM_006715990.2:c.2508+11G>A	XP_006716053.1:n.2508+11G>A
XM_006715991.2:c.2508+11G>A	XP_006716054.1:n.2508+11G>A
XM_011516223.1:c.3855+11G>A	XP_011514525.1:n.3855+11G>A
NM_000245.3:c.3798+11G>A	NP_000236.2:n.3798+11G>A
NM_001127500.2:c.3852+11G>A	NP_001120972.1:n.3852+11G>A
NM_001324402.1:c.2508+11G>A	NP_001311331.1:n.2508+11G>A
XR_001744772.1:n.3929+11G>A
NM_001127500.3:c.3852+11G>A	NP_001120972.1:n.3852+11G>A
NM_000245.4:c.3798+11G>A MANE Select	NP_000236.2:n.3798+11G>A
NM_001324402.2:c.2508+11G>A	NP_001311331.1:n.2508+11G>A