Canonical Allele Identifier: CA577680516

Gene: MET

Linked Data

• dbSNP Id: rs1487375846
• gnomAD v2: 7-116411716-T-TAGCC
• MyVariant Identifiers: chr7:g.116411716_116411717insAGCC (hg19) ; chr7:g.116771662_116771663insAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771662_116771663insAGCC , CM000669.2:g.116771662_116771663insAGCC	GRCh38
NC_000007.13:g.116411716_116411717insAGCC , CM000669.1:g.116411716_116411717insAGCC	GRCh37
NC_000007.12:g.116198952_116198953insAGCC	NCBI36
NG_008996.1:g.104258_104259insAGCC , LRG_662:g.104258_104259insAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*492+8_*492+9insAGCC	ENSP00000410980.2:n.*492+8_*492+9insAGCC
ENST00000318493.11:c.2941+8_2941+9insAGCC	ENSP00000317272.6:n.2941+8_2941+9insAGCC
ENST00000397752.8:c.2887+8_2887+9insAGCC MANE Select	ENSP00000380860.3:n.2887+8_2887+9insAGCC
ENST00000318493.10:c.2941+8_2941+9insAGCC	ENSP00000317272.6:n.2941+8_2941+9insAGCC
ENST00000397752.7:c.2887+8_2887+9insAGCC	ENSP00000380860.3:n.2887+8_2887+9insAGCC
ENST00000454623.1:c.283+8_283+9insAGCC	ENSP00000398140.1:n.283+8_283+9insAGCC
NM_000245.2:c.2887+8_2887+9insAGCC	NP_000236.2:n.2887+8_2887+9insAGCC
NM_001127500.1:c.2941+8_2941+9insAGCC , LRG_662t1:c.2941+8_2941+9insAGCC	NP_001120972.1:n.2941+8_2941+9insAGCC
XM_006715990.2:c.1597+8_1597+9insAGCC	XP_006716053.1:n.1597+8_1597+9insAGCC
XM_006715991.2:c.1597+8_1597+9insAGCC	XP_006716054.1:n.1597+8_1597+9insAGCC
XM_011516223.1:c.2944+8_2944+9insAGCC	XP_011514525.1:n.2944+8_2944+9insAGCC
NM_000245.3:c.2887+8_2887+9insAGCC	NP_000236.2:n.2887+8_2887+9insAGCC
NM_001127500.2:c.2941+8_2941+9insAGCC	NP_001120972.1:n.2941+8_2941+9insAGCC
NM_001324402.1:c.1597+8_1597+9insAGCC	NP_001311331.1:n.1597+8_1597+9insAGCC
XR_001744772.1:n.3018+8_3018+9insAGCC
NM_001127500.3:c.2941+8_2941+9insAGCC	NP_001120972.1:n.2941+8_2941+9insAGCC
NM_000245.4:c.2887+8_2887+9insAGCC MANE Select	NP_000236.2:n.2887+8_2887+9insAGCC
NM_001324402.2:c.1597+8_1597+9insAGCC	NP_001311331.1:n.1597+8_1597+9insAGCC