Canonical Allele Identifier: CA2715553266

Gene: MET

Linked Data

• dbSNP Id: rs2116995633

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771835_116771851del , CM000669.2:g.116771835_116771851del	GRCh38
NC_000007.13:g.116411889_116411905del , CM000669.1:g.116411889_116411905del	GRCh37
NC_000007.12:g.116199125_116199141del	NCBI36
NG_008996.1:g.104431_104447del , LRG_662:g.104431_104447del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-14_*495del
ENST00000318493.11:c.2942-14_2944del
ENST00000397752.8:c.2888-14_2890del
ENST00000318493.10:c.2942-14_2944del
ENST00000397752.7:c.2888-14_2890del
ENST00000454623.1:c.283+181_283+197del	ENSP00000398140.1:n.283+181_283+197del
NM_000245.2:c.2888-14_2890del
NM_001127500.1:c.2942-14_2944del , LRG_662t1:c.2942-14_2944del
XM_006715990.2:c.1598-14_1600del
XM_006715991.2:c.1598-14_1600del
XM_011516223.1:c.2945-14_2947del
NM_000245.3:c.2888-14_2890del
NM_001127500.2:c.2942-14_2944del
NM_001324402.1:c.1598-14_1600del
XR_001744772.1:n.3019-14_3021del
NM_001127500.3:c.2942-14_2944del
NM_000245.4:c.2888-14_2890del
NM_001324402.2:c.1598-14_1600del