Canonical Allele Identifier: CA2015337214

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9090019_9090026delinsATTTCCTG , CM000674.2:g.9090019_9090026delinsATTTCCTG GRCh38
NC_000012.11:g.9242615_9242622delinsATTTCCTG , CM000674.1:g.9242615_9242622delinsATTTCCTG GRCh37
NC_000012.10:g.9133882_9133889delinsATTTCCTG NCBI36
NG_011717.1:g.30937_30944delinsCAGGAAAT
NG_011717.2:g.30937_30944delinsCAGGAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.2597-3_2601delinsCAGGAAAT (A2M)
ENST00000318602.11:c.2597-3_2601delinsCAGGAAAT (A2M)
ENST00000462568.1:n.176-3_180delinsCAGGAAAT (A2M)
ENST00000543436.2:n.340-3_344delinsCAGGAAAT (A2M)
ENST00000545828.1:n.348+11524_348+11531delinsCAGGAAAT (A2M)
NM_000014.4:c.2597-3_2601delinsCAGGAAAT (A2M)
XM_006719056.2:c.2597-3_2601delinsCAGGAAAT (A2M)
NM_000014.5:c.2597-3_2601delinsCAGGAAAT (A2M)
NM_001347423.1:c.2597-3_2601delinsCAGGAAAT (A2M)
NM_001347424.1:c.2297-3_2301delinsCAGGAAAT (A2M)
NM_001347425.1:c.2147-3_2151delinsCAGGAAAT (A2M)
XM_006719056.3:c.2597-3_2601delinsCAGGAAAT (A2M)
XM_017018683.1:c.*33+31853_*33+31860delinsATTTCCTG (KLRG1) XP_016874172.1:n.*33+31853_*33+31860delinsATTTCCTG
XM_017018684.1:c.*33+31853_*33+31860delinsATTTCCTG (KLRG1) XP_016874173.1:n.*33+31853_*33+31860delinsATTTCCTG
XM_017018685.1:c.*33+31853_*33+31860delinsATTTCCTG (KLRG1) XP_016874174.1:n.*33+31853_*33+31860delinsATTTCCTG
NM_000014.6:c.2597-3_2601delinsCAGGAAAT (A2M)
NM_001347423.2:c.2597-3_2601delinsCAGGAAAT (A2M)
NM_001347424.2:c.2297-3_2301delinsCAGGAAAT (A2M)
NM_001347425.2:c.2147-3_2151delinsCAGGAAAT (A2M)