Canonical Allele Identifier: CA2684592618

Gene: MET

Linked Data

• gnomAD v4: 7-116783201-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783202_116783203del , CM000669.2:g.116783202_116783203del	GRCh38
NC_000007.13:g.116423256_116423257del , CM000669.1:g.116423256_116423257del	GRCh37
NC_000007.12:g.116210492_116210493del	NCBI36
NG_008996.1:g.115798_115799del , LRG_662:g.115798_115799del

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1238-102_*1238-101del	ENSP00000410980.2:n.*1238-102_*1238-101del
ENST00000318493.11:c.3687-102_3687-101del	ENSP00000317272.6:n.3687-102_3687-101del
ENST00000397752.8:c.3633-102_3633-101del MANE Select	ENSP00000380860.3:n.3633-102_3633-101del
ENST00000318493.10:c.3687-102_3687-101del	ENSP00000317272.6:n.3687-102_3687-101del
ENST00000397752.7:c.3633-102_3633-101del	ENSP00000380860.3:n.3633-102_3633-101del
NM_000245.2:c.3633-102_3633-101del	NP_000236.2:n.3633-102_3633-101del
NM_001127500.1:c.3687-102_3687-101del , LRG_662t1:c.3687-102_3687-101del	NP_001120972.1:n.3687-102_3687-101del
XM_006715990.2:c.2343-102_2343-101del	XP_006716053.1:n.2343-102_2343-101del
XM_006715991.2:c.2343-102_2343-101del	XP_006716054.1:n.2343-102_2343-101del
XM_011516223.1:c.3690-102_3690-101del	XP_011514525.1:n.3690-102_3690-101del
NM_000245.3:c.3633-102_3633-101del	NP_000236.2:n.3633-102_3633-101del
NM_001127500.2:c.3687-102_3687-101del	NP_001120972.1:n.3687-102_3687-101del
NM_001324402.1:c.2343-102_2343-101del	NP_001311331.1:n.2343-102_2343-101del
XR_001744772.1:n.3764-102_3764-101del
NM_001127500.3:c.3687-102_3687-101del	NP_001120972.1:n.3687-102_3687-101del
NM_000245.4:c.3633-102_3633-101del MANE Select	NP_000236.2:n.3633-102_3633-101del
NM_001324402.2:c.2343-102_2343-101del	NP_001311331.1:n.2343-102_2343-101del