Canonical Allele Identifier: CA3054204812

Gene: MET

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783290del , CM000669.2:g.116783290del	GRCh38
NC_000007.13:g.116423344del , CM000669.1:g.116423344del	GRCh37
NC_000007.12:g.116210580del	NCBI36
NG_008996.1:g.115886del , LRG_662:g.115886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1238-14del	ENSP00000410980.2:n.*1238-14del
ENST00000318493.11:c.3687-14del	ENSP00000317272.6:n.3687-14del
ENST00000397752.8:c.3633-14del MANE Select	ENSP00000380860.3:n.3633-14del
ENST00000318493.10:c.3687-14del	ENSP00000317272.6:n.3687-14del
ENST00000397752.7:c.3633-14del	ENSP00000380860.3:n.3633-14del
NM_000245.2:c.3633-14del	NP_000236.2:n.3633-14del
NM_001127500.1:c.3687-14del , LRG_662t1:c.3687-14del	NP_001120972.1:n.3687-14del
XM_006715990.2:c.2343-14del	XP_006716053.1:n.2343-14del
XM_006715991.2:c.2343-14del	XP_006716054.1:n.2343-14del
XM_011516223.1:c.3690-14del	XP_011514525.1:n.3690-14del
NM_000245.3:c.3633-14del	NP_000236.2:n.3633-14del
NM_001127500.2:c.3687-14del	NP_001120972.1:n.3687-14del
NM_001324402.1:c.2343-14del	NP_001311331.1:n.2343-14del
XR_001744772.1:n.3764-14del
NM_001127500.3:c.3687-14del	NP_001120972.1:n.3687-14del
NM_000245.4:c.3633-14del MANE Select	NP_000236.2:n.3633-14del
NM_001324402.2:c.2343-14del	NP_001311331.1:n.2343-14del