Canonical Allele Identifier: CA2617528412

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9068861_9068864del , CM000674.2:g.9068861_9068864del GRCh38
NC_000012.11:g.9221457_9221460del , CM000674.1:g.9221457_9221460del GRCh37
NC_000012.10:g.9112724_9112727del NCBI36
NG_011717.1:g.52101_52104del
NG_011717.2:g.52101_52104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.4264-20_4264-17del (A2M) MANE Select ENSP00000323929.8:n.4264-20_4264-17del
ENST00000318602.11:c.4264-20_4264-17del (A2M) ENSP00000323929.7:n.4264-20_4264-17del
ENST00000495442.1:n.94_97del (A2M)
ENST00000495709.1:n.217_220del (A2M)
ENST00000543436.2:n.452-1050_452-1047del (A2M)
NM_000014.4:c.4264-20_4264-17del (A2M) NP_000005.2:n.4264-20_4264-17del
XM_006719056.2:c.4264-20_4264-17del (A2M) XP_006719119.1:n.4264-20_4264-17del
NM_000014.5:c.4264-20_4264-17del (A2M) NP_000005.2:n.4264-20_4264-17del
NM_001347423.1:c.4264-20_4264-17del (A2M) NP_001334352.1:n.4264-20_4264-17del
NM_001347424.1:c.3964-20_3964-17del (A2M) NP_001334353.1:n.3964-20_3964-17del
NM_001347425.1:c.3814-20_3814-17del (A2M) NP_001334354.1:n.3814-20_3814-17del
XM_006719056.3:c.4264-20_4264-17del (A2M) XP_006719119.1:n.4264-20_4264-17del
XM_017018683.1:c.*33+10695_*33+10698del (KLRG1) XP_016874172.1:n.*33+10695_*33+10698del
XM_017018684.1:c.*33+10695_*33+10698del (KLRG1) XP_016874173.1:n.*33+10695_*33+10698del
XM_017018685.1:c.*33+10695_*33+10698del (KLRG1) XP_016874174.1:n.*33+10695_*33+10698del
NM_000014.6:c.4264-20_4264-17del (A2M) MANE Select NP_000005.3:n.4264-20_4264-17del
NM_001347423.2:c.4264-20_4264-17del (A2M) NP_001334352.2:n.4264-20_4264-17del
NM_001347424.2:c.3964-20_3964-17del (A2M) NP_001334353.2:n.3964-20_3964-17del
NM_001347425.2:c.3814-20_3814-17del (A2M) NP_001334354.2:n.3814-20_3814-17del