Canonical Allele Identifier: CA2015346958

Linked Data

dbSNP Id: rs1939078685

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115829_9115831del , CM000674.2:g.9115829_9115831del GRCh38
NC_000012.11:g.9268425_9268427del , CM000674.1:g.9268425_9268427del GRCh37
NC_000012.10:g.9159692_9159694del NCBI36
NG_011717.1:g.5133_5135del
NG_011717.2:g.5133_5135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.20_22del (A2M) MANE Select ENSP00000323929.8:p.Leu7del
ENST00000318602.11:c.20_22del (A2M) ENSP00000323929.7:p.Leu7del
ENST00000404455.2:c.20_22del (A2M) ENSP00000385710.2:p.Leu7del
ENST00000467091.1:n.232_234del (A2M)
ENST00000497324.1:n.188_190del (A2M)
ENST00000539638.5:c.20_22del (A2M) ENSP00000445717.1:p.Leu7del
NM_000014.4:c.20_22del (A2M) NP_000005.2:p.Leu7del
XM_006719056.2:c.20_22del (A2M) XP_006719119.1:p.Leu7del
NM_000014.5:c.20_22del (A2M) NP_000005.2:p.Leu7del
NM_001347423.1:c.20_22del (A2M) NP_001334352.1:p.Leu7del
NM_001347424.1:c.-434_-432del (A2M) NP_001334353.1:n.-434_-432del
NM_001347425.1:c.-271_-269del (A2M) NP_001334354.1:n.-271_-269del
XM_006719056.3:c.20_22del (A2M) XP_006719119.1:p.Leu7del
XM_017018683.1:c.*34-9545_*34-9543del (KLRG1) XP_016874172.1:n.*34-9545_*34-9543del
XM_017018684.1:c.*34-19257_*34-19255del (KLRG1) XP_016874173.1:n.*34-19257_*34-19255del
XM_017018685.1:c.*33+57663_*33+57665del (KLRG1) XP_016874174.1:n.*33+57663_*33+57665del
NM_000014.6:c.20_22del (A2M) MANE Select NP_000005.3:p.Leu7del
NM_001347423.2:c.20_22del (A2M) NP_001334352.2:p.Leu7del
NM_001347424.2:c.-434_-432del (A2M) NP_001334353.2:n.-434_-432del
NM_001347425.2:c.-271_-269del (A2M) NP_001334354.2:n.-271_-269del