Canonical Allele Identifier: CA2674681937

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96775533del , CM000667.2:g.96775533del GRCh38
NC_000005.9:g.96111237del , CM000667.1:g.96111237del GRCh37
NC_000005.8:g.96136993del NCBI36
NG_027839.1:g.43612del
NG_029490.1:g.118497del
NG_027839.2:g.165451del
NG_029490.2:g.118497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.*863del (ERAP1) MANE Select ENSP00000406304.2:n.*863del
ENST00000296754.7:c.2818+871del (ERAP1) ENSP00000296754.3:n.2818+871del
ENST00000443439.6:c.*863del (ERAP1) ENSP00000406304.2:n.*863del
ENST00000510098.1:c.963-1335del (CAST) ENSP00000427195.1:n.963-1335del
NM_001040458.1:c.*863del (ERAP1) NP_001035548.1:n.*863del
NM_001198541.1:c.*863del (ERAP1) NP_001185470.1:n.*863del
NM_016442.3:c.2818+871del (ERAP1) NP_057526.3:n.2818+871del
XM_005272015.3:c.2818+871del (ERAP1) XP_005272072.1:n.2818+871del
XM_005272016.3:c.2818+871del (ERAP1) XP_005272073.1:n.2818+871del
XM_011543480.1:c.2818+871del (ERAP1) XP_011541782.1:n.2818+871del
XM_011543481.1:c.2818+871del (ERAP1) XP_011541783.1:n.2818+871del
XM_011543482.1:c.2818+871del (ERAP1) XP_011541784.1:n.2818+871del
XM_011543483.1:c.2818+871del (ERAP1) XP_011541785.1:n.2818+871del
XM_011543484.1:c.2818+871del (ERAP1) XP_011541786.1:n.2818+871del
XM_011543485.1:c.2818+871del (ERAP1) XP_011541787.1:n.2818+871del
XM_011543486.1:c.*863del (ERAP1) XP_011541788.1:n.*863del
XM_011543487.1:c.2818+871del (ERAP1) XP_011541789.1:n.2818+871del
NM_001040458.2:c.*863del (ERAP1) NP_001035548.1:n.*863del
NM_001198541.2:c.*863del (ERAP1) NP_001185470.1:n.*863del
NM_001349244.1:c.2818+871del (ERAP1) NP_001336173.1:n.2818+871del
NM_016442.4:c.2818+871del (ERAP1) NP_057526.3:n.2818+871del
XM_005272015.5:c.2818+871del (ERAP1) XP_005272072.1:n.2818+871del
XM_005272016.4:c.2818+871del (ERAP1) XP_005272073.1:n.2818+871del
XM_011543480.2:c.2818+871del (ERAP1) XP_011541782.1:n.2818+871del
XM_011543481.2:c.2818+871del (ERAP1) XP_011541783.1:n.2818+871del
XM_011543484.2:c.2818+871del (ERAP1) XP_011541786.1:n.2818+871del
XM_011543485.2:c.2818+871del (ERAP1) XP_011541787.1:n.2818+871del
XM_011543486.3:c.*863del (ERAP1) XP_011541788.1:n.*863del
XM_017009581.1:c.2818+871del (ERAP1) XP_016865070.1:n.2818+871del
XM_017009583.2:c.1723+871del (ERAP1) XP_016865072.1:n.1723+871del
XM_024446113.1:c.2818+871del (ERAP1) XP_024301881.1:n.2818+871del
XR_001742119.2:n.2956+871del (ERAP1)
NM_001040458.3:c.*863del (ERAP1) MANE Select NP_001035548.1:n.*863del
NM_001198541.3:c.*863del (ERAP1) NP_001185470.1:n.*863del
NM_001349244.2:c.2818+871del (ERAP1) NP_001336173.1:n.2818+871del
NM_016442.5:c.2818+871del (ERAP1) NP_057526.3:n.2818+871del