Canonical Allele Identifier: CA2715553405

Gene: MET

Linked Data

• dbSNP Id: rs2116998072

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771989_116772009del , CM000669.2:g.116771989_116772009del	GRCh38
NC_000007.13:g.116412043_116412063del , CM000669.1:g.116412043_116412063del	GRCh37
NC_000007.12:g.116199279_116199299del	NCBI36
NG_008996.1:g.104585_104605del , LRG_662:g.104585_104605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633_*633+20del
ENST00000318493.11:c.3082_3082+20del
ENST00000397752.8:c.3028_3028+20del
ENST00000318493.10:c.3082_3082+20del
ENST00000397752.7:c.3028_3028+20del
ENST00000454623.1:c.283+335_283+355del	ENSP00000398140.1:n.283+335_283+355del
NM_000245.2:c.3028_3028+20del
NM_001127500.1:c.3082_3082+20del , LRG_662t1:c.3082_3082+20del
XM_006715990.2:c.1738_1738+20del
XM_006715991.2:c.1738_1738+20del
XM_011516223.1:c.3085_3085+20del
NM_000245.3:c.3028_3028+20del
NM_001127500.2:c.3082_3082+20del
NM_001324402.1:c.1738_1738+20del
XR_001744772.1:n.3159_3159+20del
NM_001127500.3:c.3082_3082+20del
NM_000245.4:c.3028_3028+20del
NM_001324402.2:c.1738_1738+20del