Canonical Allele Identifier: CA1565586854

Gene: ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96803330_96803334delinsACAAT , CM000667.2:g.96803330_96803334delinsACAAT	GRCh38
NC_000005.9:g.96139033_96139037delinsACAAT , CM000667.1:g.96139033_96139037delinsACAAT	GRCh37
NC_000005.8:g.96164789_96164793delinsACAAT	NCBI36
NG_027839.1:g.15812_15816delinsATTGT
NG_027839.2:g.137650_137654delinsATTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.524+69_524+73delinsATTGT MANE Select	ENSP00000406304.2:n.524+69_524+73delinsATTGT
ENST00000296754.7:c.524+69_524+73delinsATTGT	ENSP00000296754.3:n.524+69_524+73delinsATTGT
ENST00000443439.6:c.524+69_524+73delinsATTGT	ENSP00000406304.2:n.524+69_524+73delinsATTGT
ENST00000503921.5:c.-61+69_-61+73delinsATTGT	ENSP00000427025.1:n.-61+69_-61+73delinsATTGT
ENST00000508227.5:c.-41+69_-41+73delinsATTGT	ENSP00000422631.1:n.-41+69_-41+73delinsATTGT
NM_001040458.1:c.524+69_524+73delinsATTGT	NP_001035548.1:n.524+69_524+73delinsATTGT
NM_001198541.1:c.524+69_524+73delinsATTGT	NP_001185470.1:n.524+69_524+73delinsATTGT
NM_016442.3:c.524+69_524+73delinsATTGT	NP_057526.3:n.524+69_524+73delinsATTGT
XM_005272015.3:c.524+69_524+73delinsATTGT	XP_005272072.1:n.524+69_524+73delinsATTGT
XM_005272016.3:c.524+69_524+73delinsATTGT	XP_005272073.1:n.524+69_524+73delinsATTGT
XM_011543480.1:c.524+69_524+73delinsATTGT	XP_011541782.1:n.524+69_524+73delinsATTGT
XM_011543481.1:c.524+69_524+73delinsATTGT	XP_011541783.1:n.524+69_524+73delinsATTGT
XM_011543482.1:c.524+69_524+73delinsATTGT	XP_011541784.1:n.524+69_524+73delinsATTGT
XM_011543483.1:c.524+69_524+73delinsATTGT	XP_011541785.1:n.524+69_524+73delinsATTGT
XM_011543484.1:c.524+69_524+73delinsATTGT	XP_011541786.1:n.524+69_524+73delinsATTGT
XM_011543485.1:c.524+69_524+73delinsATTGT	XP_011541787.1:n.524+69_524+73delinsATTGT
XM_011543486.1:c.524+69_524+73delinsATTGT	XP_011541788.1:n.524+69_524+73delinsATTGT
XM_011543487.1:c.524+69_524+73delinsATTGT	XP_011541789.1:n.524+69_524+73delinsATTGT
NM_001040458.2:c.524+69_524+73delinsATTGT	NP_001035548.1:n.524+69_524+73delinsATTGT
NM_001198541.2:c.524+69_524+73delinsATTGT	NP_001185470.1:n.524+69_524+73delinsATTGT
NM_001349244.1:c.524+69_524+73delinsATTGT	NP_001336173.1:n.524+69_524+73delinsATTGT
NM_016442.4:c.524+69_524+73delinsATTGT	NP_057526.3:n.524+69_524+73delinsATTGT
XM_005272015.5:c.524+69_524+73delinsATTGT	XP_005272072.1:n.524+69_524+73delinsATTGT
XM_005272016.4:c.524+69_524+73delinsATTGT	XP_005272073.1:n.524+69_524+73delinsATTGT
XM_011543480.2:c.524+69_524+73delinsATTGT	XP_011541782.1:n.524+69_524+73delinsATTGT
XM_011543481.2:c.524+69_524+73delinsATTGT	XP_011541783.1:n.524+69_524+73delinsATTGT
XM_011543484.2:c.524+69_524+73delinsATTGT	XP_011541786.1:n.524+69_524+73delinsATTGT
XM_011543485.2:c.524+69_524+73delinsATTGT	XP_011541787.1:n.524+69_524+73delinsATTGT
XM_011543486.3:c.524+69_524+73delinsATTGT	XP_011541788.1:n.524+69_524+73delinsATTGT
XM_017009581.1:c.524+69_524+73delinsATTGT	XP_016865070.1:n.524+69_524+73delinsATTGT
XM_017009583.2:c.-519+69_-519+73delinsATTGT	XP_016865072.1:n.-519+69_-519+73delinsATTGT
XM_024446113.1:c.524+69_524+73delinsATTGT	XP_024301881.1:n.524+69_524+73delinsATTGT
XR_001742119.2:n.817+69_817+73delinsATTGT
NM_001040458.3:c.524+69_524+73delinsATTGT MANE Select	NP_001035548.1:n.524+69_524+73delinsATTGT
NM_001198541.3:c.524+69_524+73delinsATTGT	NP_001185470.1:n.524+69_524+73delinsATTGT
NM_001349244.2:c.524+69_524+73delinsATTGT	NP_001336173.1:n.524+69_524+73delinsATTGT
NM_016442.5:c.524+69_524+73delinsATTGT	NP_057526.3:n.524+69_524+73delinsATTGT