Canonical Allele Identifier: CA645567308

Gene: MET

Linked Data

• COSMIC: COSM13245 ; COSM29632

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771849_116771989del , CM000669.2:g.116771849_116771989del	GRCh38
NC_000007.13:g.116411903_116412043del , CM000669.1:g.116411903_116412043del	GRCh37
NC_000007.12:g.116199139_116199279del	NCBI36
NG_008996.1:g.104445_104585del , LRG_662:g.104445_104585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493_*633del
ENST00000318493.11:c.2942_3082del
ENST00000397752.8:c.2888_3028del
ENST00000318493.10:c.2942_3082del
ENST00000397752.7:c.2888_3028del
ENST00000454623.1:c.283+195_283+335del	ENSP00000398140.1:n.283+195_283+335del
NM_000245.2:c.2888_3028del
NM_001127500.1:c.2942_3082del , LRG_662t1:c.2942_3082del
XM_006715990.2:c.1598_1738del
XM_006715991.2:c.1598_1738del
XM_011516223.1:c.2945_3085del
NM_000245.3:c.2888_3028del
NM_001127500.2:c.2942_3082del
NM_001324402.1:c.1598_1738del
XR_001744772.1:n.3019_3159del
NM_001127500.3:c.2942_3082del
NM_000245.4:c.2888_3028del
NM_001324402.2:c.1598_1738del