Canonical Allele Identifier: CA1737037479

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771696_116771698delinsAAC , CM000669.2:g.116771696_116771698delinsAAC	GRCh38
NC_000007.13:g.116411750_116411752delinsAAC , CM000669.1:g.116411750_116411752delinsAAC	GRCh37
NC_000007.12:g.116198986_116198988delinsAAC	NCBI36
NG_008996.1:g.104292_104294delinsAAC , LRG_662:g.104292_104294delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*492+42_*492+44delinsAAC	ENSP00000410980.2:n.*492+42_*492+44delinsAAC
ENST00000318493.11:c.2941+42_2941+44delinsAAC	ENSP00000317272.6:n.2941+42_2941+44delinsAAC
ENST00000397752.8:c.2887+42_2887+44delinsAAC MANE Select	ENSP00000380860.3:n.2887+42_2887+44delinsAAC
ENST00000318493.10:c.2941+42_2941+44delinsAAC	ENSP00000317272.6:n.2941+42_2941+44delinsAAC
ENST00000397752.7:c.2887+42_2887+44delinsAAC	ENSP00000380860.3:n.2887+42_2887+44delinsAAC
ENST00000454623.1:c.283+42_283+44delinsAAC	ENSP00000398140.1:n.283+42_283+44delinsAAC
NM_000245.2:c.2887+42_2887+44delinsAAC	NP_000236.2:n.2887+42_2887+44delinsAAC
NM_001127500.1:c.2941+42_2941+44delinsAAC , LRG_662t1:c.2941+42_2941+44delinsAAC	NP_001120972.1:n.2941+42_2941+44delinsAAC
XM_006715990.2:c.1597+42_1597+44delinsAAC	XP_006716053.1:n.1597+42_1597+44delinsAAC
XM_006715991.2:c.1597+42_1597+44delinsAAC	XP_006716054.1:n.1597+42_1597+44delinsAAC
XM_011516223.1:c.2944+42_2944+44delinsAAC	XP_011514525.1:n.2944+42_2944+44delinsAAC
NM_000245.3:c.2887+42_2887+44delinsAAC	NP_000236.2:n.2887+42_2887+44delinsAAC
NM_001127500.2:c.2941+42_2941+44delinsAAC	NP_001120972.1:n.2941+42_2941+44delinsAAC
NM_001324402.1:c.1597+42_1597+44delinsAAC	NP_001311331.1:n.1597+42_1597+44delinsAAC
XR_001744772.1:n.3018+42_3018+44delinsAAC
NM_001127500.3:c.2941+42_2941+44delinsAAC	NP_001120972.1:n.2941+42_2941+44delinsAAC
NM_000245.4:c.2887+42_2887+44delinsAAC MANE Select	NP_000236.2:n.2887+42_2887+44delinsAAC
NM_001324402.2:c.1597+42_1597+44delinsAAC	NP_001311331.1:n.1597+42_1597+44delinsAAC