Canonical Allele Identifier: CA2573334445
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771833_116771863delinsC , CM000669.2:g.116771833_116771863delinsC GRCh38
NC_000007.13:g.116411887_116411917delinsC , CM000669.1:g.116411887_116411917delinsC GRCh37
NC_000007.12:g.116199123_116199153delinsC NCBI36
NG_008996.1:g.104429_104459delinsC , LRG_662:g.104429_104459delinsC

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*493-16_*507delinsC
ENST00000318493.11:c.2942-16_2956delinsC
ENST00000397752.8:c.2888-16_2902delinsC
ENST00000318493.10:c.2942-16_2956delinsC
ENST00000397752.7:c.2888-16_2902delinsC
ENST00000454623.1:c.283+179_283+209delinsC ENSP00000398140.1:n.283+179_283+209delinsC
NM_000245.2:c.2888-16_2902delinsC
NM_001127500.1:c.2942-16_2956delinsC , LRG_662t1:c.2942-16_2956delinsC
XM_006715990.2:c.1598-16_1612delinsC
XM_006715991.2:c.1598-16_1612delinsC
XM_011516223.1:c.2945-16_2959delinsC
NM_000245.3:c.2888-16_2902delinsC
NM_001127500.2:c.2942-16_2956delinsC
NM_001324402.1:c.1598-16_1612delinsC
XR_001744772.1:n.3019-16_3033delinsC
NM_001127500.3:c.2942-16_2956delinsC
NM_000245.4:c.2888-16_2902delinsC
NM_001324402.2:c.1598-16_1612delinsC