Canonical Allele Identifier: CA2715553276
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116995750

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771844_116771851delinsATA , CM000669.2:g.116771844_116771851delinsATA GRCh38
NC_000007.13:g.116411898_116411905delinsATA , CM000669.1:g.116411898_116411905delinsATA GRCh37
NC_000007.12:g.116199134_116199141delinsATA NCBI36
NG_008996.1:g.104440_104447delinsATA , LRG_662:g.104440_104447delinsATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*493-5_*495delinsATA
ENST00000318493.11:c.2942-5_2944delinsATA
ENST00000397752.8:c.2888-5_2890delinsATA
ENST00000318493.10:c.2942-5_2944delinsATA
ENST00000397752.7:c.2888-5_2890delinsATA
ENST00000454623.1:c.283+190_283+197delinsATA ENSP00000398140.1:n.283+190_283+197delinsATA
NM_000245.2:c.2888-5_2890delinsATA
NM_001127500.1:c.2942-5_2944delinsATA , LRG_662t1:c.2942-5_2944delinsATA
XM_006715990.2:c.1598-5_1600delinsATA
XM_006715991.2:c.1598-5_1600delinsATA
XM_011516223.1:c.2945-5_2947delinsATA
NM_000245.3:c.2888-5_2890delinsATA
NM_001127500.2:c.2942-5_2944delinsATA
NM_001324402.1:c.1598-5_1600delinsATA
XR_001744772.1:n.3019-5_3021delinsATA
NM_001127500.3:c.2942-5_2944delinsATA
NM_000245.4:c.2888-5_2890delinsATA
NM_001324402.2:c.1598-5_1600delinsATA