Canonical Allele Identifier: CA2573332098

Gene: MET

Linked Data

• CIViC: CA2573332098

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771839_116771872del , CM000669.2:g.116771839_116771872del	GRCh38
NC_000007.13:g.116411893_116411926del , CM000669.1:g.116411893_116411926del	GRCh37
NC_000007.12:g.116199129_116199162del	NCBI36
NG_008996.1:g.104435_104468del , LRG_662:g.104435_104468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-10_*516del
ENST00000318493.11:c.2942-10_2965del
ENST00000397752.8:c.2888-10_2911del
ENST00000318493.10:c.2942-10_2965del
ENST00000397752.7:c.2888-10_2911del
ENST00000454623.1:c.283+185_283+218del	ENSP00000398140.1:n.283+185_283+218del
NM_000245.2:c.2888-10_2911del
NM_001127500.1:c.2942-10_2965del , LRG_662t1:c.2942-10_2965del
XM_006715990.2:c.1598-10_1621del
XM_006715991.2:c.1598-10_1621del
XM_011516223.1:c.2945-10_2968del
NM_000245.3:c.2888-10_2911del
NM_001127500.2:c.2942-10_2965del
NM_001324402.1:c.1598-10_1621del
XR_001744772.1:n.3019-10_3042del
NM_001127500.3:c.2942-10_2965del
NM_000245.4:c.2888-10_2911del
NM_001324402.2:c.1598-10_1621del