Canonical Allele Identifier: CA1565575928

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96775260_96775261delinsTC , CM000667.2:g.96775260_96775261delinsTC GRCh38
NC_000005.9:g.96110964_96110965delinsTC , CM000667.1:g.96110964_96110965delinsTC GRCh37
NC_000005.8:g.96136720_96136721delinsTC NCBI36
NG_027839.1:g.43884_43885delinsGA
NG_029490.1:g.118224_118225delinsTC
NG_027839.2:g.165723_165724delinsGA
NG_029490.2:g.118224_118225delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.*1135_*1136delinsGA (ERAP1) MANE Select ENSP00000406304.2:n.*1135_*1136delinsGA
ENST00000296754.7:c.2818+1143_2818+1144delinsGA (ERAP1) ENSP00000296754.3:n.2818+1143_2818+1144delinsGA
ENST00000443439.6:c.*1135_*1136delinsGA (ERAP1) ENSP00000406304.2:n.*1135_*1136delinsGA
ENST00000510098.1:c.963-1608_963-1607delinsTC (CAST) ENSP00000427195.1:n.963-1608_963-1607delinsTC
NM_001040458.1:c.*1135_*1136delinsGA (ERAP1) NP_001035548.1:n.*1135_*1136delinsGA
NM_001198541.1:c.*1135_*1136delinsGA (ERAP1) NP_001185470.1:n.*1135_*1136delinsGA
NM_016442.3:c.2818+1143_2818+1144delinsGA (ERAP1) NP_057526.3:n.2818+1143_2818+1144delinsGA
XM_005272015.3:c.2818+1143_2818+1144delinsGA (ERAP1) XP_005272072.1:n.2818+1143_2818+1144delinsGA
XM_005272016.3:c.2818+1143_2818+1144delinsGA (ERAP1) XP_005272073.1:n.2818+1143_2818+1144delinsGA
XM_011543480.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541782.1:n.2818+1143_2818+1144delinsGA
XM_011543481.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541783.1:n.2818+1143_2818+1144delinsGA
XM_011543482.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541784.1:n.2818+1143_2818+1144delinsGA
XM_011543483.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541785.1:n.2818+1143_2818+1144delinsGA
XM_011543484.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541786.1:n.2818+1143_2818+1144delinsGA
XM_011543485.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541787.1:n.2818+1143_2818+1144delinsGA
XM_011543486.1:c.*1135_*1136delinsGA (ERAP1) XP_011541788.1:n.*1135_*1136delinsGA
XM_011543487.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541789.1:n.2818+1143_2818+1144delinsGA
NM_001040458.2:c.*1135_*1136delinsGA (ERAP1) NP_001035548.1:n.*1135_*1136delinsGA
NM_001198541.2:c.*1135_*1136delinsGA (ERAP1) NP_001185470.1:n.*1135_*1136delinsGA
NM_001349244.1:c.2818+1143_2818+1144delinsGA (ERAP1) NP_001336173.1:n.2818+1143_2818+1144delinsGA
NM_016442.4:c.2818+1143_2818+1144delinsGA (ERAP1) NP_057526.3:n.2818+1143_2818+1144delinsGA
XM_005272015.5:c.2818+1143_2818+1144delinsGA (ERAP1) XP_005272072.1:n.2818+1143_2818+1144delinsGA
XM_005272016.4:c.2818+1143_2818+1144delinsGA (ERAP1) XP_005272073.1:n.2818+1143_2818+1144delinsGA
XM_011543480.2:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541782.1:n.2818+1143_2818+1144delinsGA
XM_011543481.2:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541783.1:n.2818+1143_2818+1144delinsGA
XM_011543484.2:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541786.1:n.2818+1143_2818+1144delinsGA
XM_011543485.2:c.2818+1143_2818+1144delinsGA (ERAP1) XP_011541787.1:n.2818+1143_2818+1144delinsGA
XM_011543486.3:c.*1135_*1136delinsGA (ERAP1) XP_011541788.1:n.*1135_*1136delinsGA
XM_017009581.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_016865070.1:n.2818+1143_2818+1144delinsGA
XM_017009583.2:c.1723+1143_1723+1144delinsGA (ERAP1) XP_016865072.1:n.1723+1143_1723+1144delinsGA
XM_024446113.1:c.2818+1143_2818+1144delinsGA (ERAP1) XP_024301881.1:n.2818+1143_2818+1144delinsGA
XR_001742119.2:n.2956+1143_2956+1144delinsGA (ERAP1)
NM_001040458.3:c.*1135_*1136delinsGA (ERAP1) MANE Select NP_001035548.1:n.*1135_*1136delinsGA
NM_001198541.3:c.*1135_*1136delinsGA (ERAP1) NP_001185470.1:n.*1135_*1136delinsGA
NM_001349244.2:c.2818+1143_2818+1144delinsGA (ERAP1) NP_001336173.1:n.2818+1143_2818+1144delinsGA
NM_016442.5:c.2818+1143_2818+1144delinsGA (ERAP1) NP_057526.3:n.2818+1143_2818+1144delinsGA