Canonical Allele Identifier: CA658821504

Gene: MET

Linked Data

• ClinVar Variation Id: 545898
• ClinVar RCV Id: RCV000657505 ; RCV003163027
• dbSNP Id: rs1554395864
• MyVariant Identifiers: chr7:g.116399403del (hg19) ; chr7:g.116759349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759349del , CM000669.2:g.116759349del	GRCh38
NC_000007.13:g.116399403del , CM000669.1:g.116399403del	GRCh37
NC_000007.12:g.116186639del	NCBI36
NG_008996.1:g.91945del , LRG_662:g.91945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2265-42del	ENSP00000398776.2:n.2265-42del
ENST00000436117.3:c.2264+729del	ENSP00000410980.2:n.2264+729del
ENST00000318493.11:c.2277del	ENSP00000317272.6:p.Glu760AsnfsTer19
ENST00000397752.8:c.2265-42del MANE Select	ENSP00000380860.3:n.2265-42del
ENST00000318493.10:c.2277del	ENSP00000317272.6:p.Glu760AsnfsTer19
ENST00000397752.7:c.2265-42del	ENSP00000380860.3:n.2265-42del
ENST00000422097.1:c.105-42del	ENSP00000398776.1:n.105-42del
ENST00000436117.2:c.2264+729del	ENSP00000410980.2:n.2264+729del
NM_000245.2:c.2265-42del	NP_000236.2:n.2265-42del
NM_001127500.1:c.2277del , LRG_662t1:c.2277del	NP_001120972.1:p.Glu760AsnfsTer19
XM_006715990.2:c.975-42del	XP_006716053.1:n.975-42del
XM_006715991.2:c.975-42del	XP_006716054.1:n.975-42del
XM_011516223.1:c.2322-42del	XP_011514525.1:n.2322-42del
NM_000245.3:c.2265-42del	NP_000236.2:n.2265-42del
NM_001127500.2:c.2277del	NP_001120972.1:p.Glu760AsnfsTer19
NM_001324401.1:c.2265-42del	NP_001311330.1:n.2265-42del
NM_001324402.1:c.975-42del	NP_001311331.1:n.975-42del
XR_001744772.1:n.2495+729del
NM_001127500.3:c.2277del	NP_001120972.1:p.Glu760AsnfsTer19
NM_000245.4:c.2265-42del MANE Select	NP_000236.2:n.2265-42del
NM_001324401.2:c.2265-42del	NP_001311330.1:n.2265-42del
NM_001324402.2:c.975-42del	NP_001311331.1:n.975-42del
NM_001324401.3:c.2265-42del	NP_001311330.1:n.2265-42del