Canonical Allele Identifier: CA2580617368
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116995750

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771844_116771851delinsA , CM000669.2:g.116771844_116771851delinsA GRCh38
NC_000007.13:g.116411898_116411905delinsA , CM000669.1:g.116411898_116411905delinsA GRCh37
NC_000007.12:g.116199134_116199141delinsA NCBI36
NG_008996.1:g.104440_104447delinsA , LRG_662:g.104440_104447delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*493-5_*495delinsA
ENST00000318493.11:c.2942-5_2944delinsA
ENST00000397752.8:c.2888-5_2890delinsA
ENST00000318493.10:c.2942-5_2944delinsA
ENST00000397752.7:c.2888-5_2890delinsA
ENST00000454623.1:c.283+190_283+197delinsA ENSP00000398140.1:n.283+190_283+197delinsA
NM_000245.2:c.2888-5_2890delinsA
NM_001127500.1:c.2942-5_2944delinsA , LRG_662t1:c.2942-5_2944delinsA
XM_006715990.2:c.1598-5_1600delinsA
XM_006715991.2:c.1598-5_1600delinsA
XM_011516223.1:c.2945-5_2947delinsA
NM_000245.3:c.2888-5_2890delinsA
NM_001127500.2:c.2942-5_2944delinsA
NM_001324402.1:c.1598-5_1600delinsA
XR_001744772.1:n.3019-5_3021delinsA
NM_001127500.3:c.2942-5_2944delinsA
NM_000245.4:c.2888-5_2890delinsA
NM_001324402.2:c.1598-5_1600delinsA