Canonical Allele Identifier: CA2831116708

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771834_116771837delinsAGA , CM000669.2:g.116771834_116771837delinsAGA	GRCh38
NC_000007.13:g.116411888_116411891delinsAGA , CM000669.1:g.116411888_116411891delinsAGA	GRCh37
NC_000007.12:g.116199124_116199127delinsAGA	NCBI36
NG_008996.1:g.104430_104433delinsAGA , LRG_662:g.104430_104433delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-15_*493-12delinsAGA	ENSP00000410980.2:n.*493-15_*493-12delinsAGA
ENST00000318493.11:c.2942-15_2942-12delinsAGA	ENSP00000317272.6:n.2942-15_2942-12delinsAGA
ENST00000397752.8:c.2888-15_2888-12delinsAGA MANE Select	ENSP00000380860.3:n.2888-15_2888-12delinsAGA
ENST00000318493.10:c.2942-15_2942-12delinsAGA	ENSP00000317272.6:n.2942-15_2942-12delinsAGA
ENST00000397752.7:c.2888-15_2888-12delinsAGA	ENSP00000380860.3:n.2888-15_2888-12delinsAGA
ENST00000454623.1:c.283+180_283+183delinsAGA	ENSP00000398140.1:n.283+180_283+183delinsAGA
NM_000245.2:c.2888-15_2888-12delinsAGA	NP_000236.2:n.2888-15_2888-12delinsAGA
NM_001127500.1:c.2942-15_2942-12delinsAGA , LRG_662t1:c.2942-15_2942-12delinsAGA	NP_001120972.1:n.2942-15_2942-12delinsAGA
XM_006715990.2:c.1598-15_1598-12delinsAGA	XP_006716053.1:n.1598-15_1598-12delinsAGA
XM_006715991.2:c.1598-15_1598-12delinsAGA	XP_006716054.1:n.1598-15_1598-12delinsAGA
XM_011516223.1:c.2945-15_2945-12delinsAGA	XP_011514525.1:n.2945-15_2945-12delinsAGA
NM_000245.3:c.2888-15_2888-12delinsAGA	NP_000236.2:n.2888-15_2888-12delinsAGA
NM_001127500.2:c.2942-15_2942-12delinsAGA	NP_001120972.1:n.2942-15_2942-12delinsAGA
NM_001324402.1:c.1598-15_1598-12delinsAGA	NP_001311331.1:n.1598-15_1598-12delinsAGA
XR_001744772.1:n.3019-15_3019-12delinsAGA
NM_001127500.3:c.2942-15_2942-12delinsAGA	NP_001120972.1:n.2942-15_2942-12delinsAGA
NM_000245.4:c.2888-15_2888-12delinsAGA MANE Select	NP_000236.2:n.2888-15_2888-12delinsAGA
NM_001324402.2:c.1598-15_1598-12delinsAGA	NP_001311331.1:n.1598-15_1598-12delinsAGA