Canonical Allele Identifier: CA2741228402

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9079831_9079832insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC , CM000674.2:g.9079831_9079832insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC	GRCh38
NC_000012.11:g.9232427_9232428insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC , CM000674.1:g.9232427_9232428insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC	GRCh37
NC_000012.10:g.9123694_9123695insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC	NCBI36
NG_011717.1:g.41131_41132insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG
NG_011717.2:g.41131_41132insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M) MANE Select	ENSP00000323929.8:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTC...
ENST00000318602.11:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	ENSP00000323929.7:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTC...
ENST00000542567.1:n.210-17_210-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)
ENST00000543436.2:n.451+10080_451+10081insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)
ENST00000545828.1:n.349-7111_349-7110insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)
NM_000014.4:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_000005.2:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTA...
XM_006719056.2:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	XP_006719119.1:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTAT...
NM_000014.5:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_000005.2:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTA...
NM_001347423.1:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334352.1:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTAT...
NM_001347424.1:c.2555-17_2555-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334353.1:n.2555-17_2555-16insGGTCTTCAATTCTACATGACCTCTAT...
NM_001347425.1:c.2405-17_2405-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334354.1:n.2405-17_2405-16insGGTCTTCAATTCTACATGACCTCTAT...
XM_006719056.3:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	XP_006719119.1:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTAT...
XM_017018683.1:c.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC (KLRG1)	XP_016874172.1:n.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTAT...
XM_017018684.1:c.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC (KLRG1)	XP_016874173.1:n.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTAT...
XM_017018685.1:c.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTATCTAAATAGAGGTCATGTAGAATTGAAGACC (KLRG1)	XP_016874174.1:n.*33+21665_*33+21666insCGCATTCGCTATTTTCCAGTAT...
NM_000014.6:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M) MANE Select	NP_000005.3:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTA...
NM_001347423.2:c.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334352.2:n.2855-17_2855-16insGGTCTTCAATTCTACATGACCTCTAT...
NM_001347424.2:c.2555-17_2555-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334353.2:n.2555-17_2555-16insGGTCTTCAATTCTACATGACCTCTAT...
NM_001347425.2:c.2405-17_2405-16insGGTCTTCAATTCTACATGACCTCTATTTAGATACTGGAAAATAGCGAATGCG (A2M)	NP_001334354.2:n.2405-17_2405-16insGGTCTTCAATTCTACATGACCTCTAT...