Canonical Allele Identifier: CA2573332831

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771836_116771872delinsC , CM000669.2:g.116771836_116771872delinsC	GRCh38
NC_000007.13:g.116411890_116411926delinsC , CM000669.1:g.116411890_116411926delinsC	GRCh37
NC_000007.12:g.116199126_116199162delinsC	NCBI36
NG_008996.1:g.104432_104468delinsC , LRG_662:g.104432_104468delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-13_*516delinsC
ENST00000318493.11:c.2942-13_2965delinsC
ENST00000397752.8:c.2888-13_2911delinsC
ENST00000318493.10:c.2942-13_2965delinsC
ENST00000397752.7:c.2888-13_2911delinsC
ENST00000454623.1:c.283+182_283+218delinsC	ENSP00000398140.1:n.283+182_283+218delinsC
NM_000245.2:c.2888-13_2911delinsC
NM_001127500.1:c.2942-13_2965delinsC , LRG_662t1:c.2942-13_2965delinsC
XM_006715990.2:c.1598-13_1621delinsC
XM_006715991.2:c.1598-13_1621delinsC
XM_011516223.1:c.2945-13_2968delinsC
NM_000245.3:c.2888-13_2911delinsC
NM_001127500.2:c.2942-13_2965delinsC
NM_001324402.1:c.1598-13_1621delinsC
XR_001744772.1:n.3019-13_3042delinsC
NM_001127500.3:c.2942-13_2965delinsC
NM_000245.4:c.2888-13_2911delinsC
NM_001324402.2:c.1598-13_1621delinsC