Canonical Allele Identifier: CA577214740

Gene: MET

Linked Data

• ClinVar Variation Id: 1603486
• ClinVar RCV Id: RCV002142076
• dbSNP Id: rs1422359365
• gnomAD v2: 7-116399550-TC-T
• gnomAD v4: 7-116759496-TC-T
• MyVariant Identifiers: chr7:g.116399551del (hg19) ; chr7:g.116759497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759498del , CM000669.2:g.116759498del	GRCh38
NC_000007.13:g.116399552del , CM000669.1:g.116399552del	GRCh37
NC_000007.12:g.116186788del	NCBI36
NG_008996.1:g.92094del , LRG_662:g.92094del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2364+8del	ENSP00000398776.2:n.2364+8del
ENST00000436117.3:c.2264+878del	ENSP00000410980.2:n.2264+878del
ENST00000318493.11:c.2418+8del	ENSP00000317272.6:n.2418+8del
ENST00000397752.8:c.2364+8del MANE Select	ENSP00000380860.3:n.2364+8del
ENST00000318493.10:c.2418+8del	ENSP00000317272.6:n.2418+8del
ENST00000397752.7:c.2364+8del	ENSP00000380860.3:n.2364+8del
ENST00000422097.1:c.204+8del	ENSP00000398776.1:n.204+8del
ENST00000436117.2:c.2264+878del	ENSP00000410980.2:n.2264+878del
NM_000245.2:c.2364+8del	NP_000236.2:n.2364+8del
NM_001127500.1:c.2418+8del , LRG_662t1:c.2418+8del	NP_001120972.1:n.2418+8del
XM_006715990.2:c.1074+8del	XP_006716053.1:n.1074+8del
XM_006715991.2:c.1074+8del	XP_006716054.1:n.1074+8del
XM_011516223.1:c.2421+8del	XP_011514525.1:n.2421+8del
NM_000245.3:c.2364+8del	NP_000236.2:n.2364+8del
NM_001127500.2:c.2418+8del	NP_001120972.1:n.2418+8del
NM_001324401.1:c.2364+8del	NP_001311330.1:n.2364+8del
NM_001324402.1:c.1074+8del	NP_001311331.1:n.1074+8del
XR_001744772.1:n.2495+878del
NM_001127500.3:c.2418+8del	NP_001120972.1:n.2418+8del
NM_000245.4:c.2364+8del MANE Select	NP_000236.2:n.2364+8del
NM_001324401.2:c.2364+8del	NP_001311330.1:n.2364+8del
NM_001324402.2:c.1074+8del	NP_001311331.1:n.1074+8del
NM_001324401.3:c.2364+8del	NP_001311330.1:n.2364+8del