Canonical Allele Identifier: CA2715553262
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116995608

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771834_116771852del , CM000669.2:g.116771834_116771852del GRCh38
NC_000007.13:g.116411888_116411906del , CM000669.1:g.116411888_116411906del GRCh37
NC_000007.12:g.116199124_116199142del NCBI36
NG_008996.1:g.104430_104448del , LRG_662:g.104430_104448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*493-15_*496del
ENST00000318493.11:c.2942-15_2945del
ENST00000397752.8:c.2888-15_2891del
ENST00000318493.10:c.2942-15_2945del
ENST00000397752.7:c.2888-15_2891del
ENST00000454623.1:c.283+180_283+198del ENSP00000398140.1:n.283+180_283+198del
NM_000245.2:c.2888-15_2891del
NM_001127500.1:c.2942-15_2945del , LRG_662t1:c.2942-15_2945del
XM_006715990.2:c.1598-15_1601del
XM_006715991.2:c.1598-15_1601del
XM_011516223.1:c.2945-15_2948del
NM_000245.3:c.2888-15_2891del
NM_001127500.2:c.2942-15_2945del
NM_001324402.1:c.1598-15_1601del
XR_001744772.1:n.3019-15_3022del
NM_001127500.3:c.2942-15_2945del
NM_000245.4:c.2888-15_2891del
NM_001324402.2:c.1598-15_1601del