Canonical Allele Identifier: CA2573332171
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771843_116771870delinsA , CM000669.2:g.116771843_116771870delinsA GRCh38
NC_000007.13:g.116411897_116411924delinsA , CM000669.1:g.116411897_116411924delinsA GRCh37
NC_000007.12:g.116199133_116199160delinsA NCBI36
NG_008996.1:g.104439_104466delinsA , LRG_662:g.104439_104466delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*493-6_*514delinsA
ENST00000318493.11:c.2942-6_2963delinsA
ENST00000397752.8:c.2888-6_2909delinsA
ENST00000318493.10:c.2942-6_2963delinsA
ENST00000397752.7:c.2888-6_2909delinsA
ENST00000454623.1:c.283+189_283+216delinsA ENSP00000398140.1:n.283+189_283+216delinsA
NM_000245.2:c.2888-6_2909delinsA
NM_001127500.1:c.2942-6_2963delinsA , LRG_662t1:c.2942-6_2963delinsA
XM_006715990.2:c.1598-6_1619delinsA
XM_006715991.2:c.1598-6_1619delinsA
XM_011516223.1:c.2945-6_2966delinsA
NM_000245.3:c.2888-6_2909delinsA
NM_001127500.2:c.2942-6_2963delinsA
NM_001324402.1:c.1598-6_1619delinsA
XR_001744772.1:n.3019-6_3040delinsA
NM_001127500.3:c.2942-6_2963delinsA
NM_000245.4:c.2888-6_2909delinsA
NM_001324402.2:c.1598-6_1619delinsA