Canonical Allele Identifier: CA164904971

Gene: MET

Linked Data

• dbSNP Id: rs869136712
• MyVariant Identifiers: chr7:g.116411851_116411852insCT (hg19) ; chr7:g.116771797_116771798insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771797_116771798insCT , CM000669.2:g.116771797_116771798insCT	GRCh38
NC_000007.13:g.116411851_116411852insCT , CM000669.1:g.116411851_116411852insCT	GRCh37
NC_000007.12:g.116199087_116199088insCT	NCBI36
NG_008996.1:g.104393_104394insCT , LRG_662:g.104393_104394insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-52_*493-51insCT	ENSP00000410980.2:n.*493-52_*493-51insCT
ENST00000318493.11:c.2942-52_2942-51insCT	ENSP00000317272.6:n.2942-52_2942-51insCT
ENST00000397752.8:c.2888-52_2888-51insCT MANE Select	ENSP00000380860.3:n.2888-52_2888-51insCT
ENST00000318493.10:c.2942-52_2942-51insCT	ENSP00000317272.6:n.2942-52_2942-51insCT
ENST00000397752.7:c.2888-52_2888-51insCT	ENSP00000380860.3:n.2888-52_2888-51insCT
ENST00000454623.1:c.283+143_283+144insCT	ENSP00000398140.1:n.283+143_283+144insCT
NM_000245.2:c.2888-52_2888-51insCT	NP_000236.2:n.2888-52_2888-51insCT
NM_001127500.1:c.2942-52_2942-51insCT , LRG_662t1:c.2942-52_2942-51insCT	NP_001120972.1:n.2942-52_2942-51insCT
XM_006715990.2:c.1598-52_1598-51insCT	XP_006716053.1:n.1598-52_1598-51insCT
XM_006715991.2:c.1598-52_1598-51insCT	XP_006716054.1:n.1598-52_1598-51insCT
XM_011516223.1:c.2945-52_2945-51insCT	XP_011514525.1:n.2945-52_2945-51insCT
NM_000245.3:c.2888-52_2888-51insCT	NP_000236.2:n.2888-52_2888-51insCT
NM_001127500.2:c.2942-52_2942-51insCT	NP_001120972.1:n.2942-52_2942-51insCT
NM_001324402.1:c.1598-52_1598-51insCT	NP_001311331.1:n.1598-52_1598-51insCT
XR_001744772.1:n.3019-52_3019-51insCT
NM_001127500.3:c.2942-52_2942-51insCT	NP_001120972.1:n.2942-52_2942-51insCT
NM_000245.4:c.2888-52_2888-51insCT MANE Select	NP_000236.2:n.2888-52_2888-51insCT
NM_001324402.2:c.1598-52_1598-51insCT	NP_001311331.1:n.1598-52_1598-51insCT