Canonical Allele Identifier: CA2674685511
Gene: ERAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96803398_96803399dup , CM000667.2:g.96803398_96803399dup GRCh38
NC_000005.9:g.96139101_96139102dup , CM000667.1:g.96139101_96139102dup GRCh37
NC_000005.8:g.96164857_96164858dup NCBI36
NG_027839.1:g.15754_15755dup
NG_027839.2:g.137592_137593dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.524+11_524+12dup MANE Select ENSP00000406304.2:n.524+11_524+12dup
ENST00000296754.7:c.524+11_524+12dup ENSP00000296754.3:n.524+11_524+12dup
ENST00000443439.6:c.524+11_524+12dup ENSP00000406304.2:n.524+11_524+12dup
ENST00000503921.5:c.-61+11_-61+12dup ENSP00000427025.1:n.-61+11_-61+12dup
ENST00000508227.5:c.-41+11_-41+12dup ENSP00000422631.1:n.-41+11_-41+12dup
NM_001040458.1:c.524+11_524+12dup NP_001035548.1:n.524+11_524+12dup
NM_001198541.1:c.524+11_524+12dup NP_001185470.1:n.524+11_524+12dup
NM_016442.3:c.524+11_524+12dup NP_057526.3:n.524+11_524+12dup
XM_005272015.3:c.524+11_524+12dup XP_005272072.1:n.524+11_524+12dup
XM_005272016.3:c.524+11_524+12dup XP_005272073.1:n.524+11_524+12dup
XM_011543480.1:c.524+11_524+12dup XP_011541782.1:n.524+11_524+12dup
XM_011543481.1:c.524+11_524+12dup XP_011541783.1:n.524+11_524+12dup
XM_011543482.1:c.524+11_524+12dup XP_011541784.1:n.524+11_524+12dup
XM_011543483.1:c.524+11_524+12dup XP_011541785.1:n.524+11_524+12dup
XM_011543484.1:c.524+11_524+12dup XP_011541786.1:n.524+11_524+12dup
XM_011543485.1:c.524+11_524+12dup XP_011541787.1:n.524+11_524+12dup
XM_011543486.1:c.524+11_524+12dup XP_011541788.1:n.524+11_524+12dup
XM_011543487.1:c.524+11_524+12dup XP_011541789.1:n.524+11_524+12dup
NM_001040458.2:c.524+11_524+12dup NP_001035548.1:n.524+11_524+12dup
NM_001198541.2:c.524+11_524+12dup NP_001185470.1:n.524+11_524+12dup
NM_001349244.1:c.524+11_524+12dup NP_001336173.1:n.524+11_524+12dup
NM_016442.4:c.524+11_524+12dup NP_057526.3:n.524+11_524+12dup
XM_005272015.5:c.524+11_524+12dup XP_005272072.1:n.524+11_524+12dup
XM_005272016.4:c.524+11_524+12dup XP_005272073.1:n.524+11_524+12dup
XM_011543480.2:c.524+11_524+12dup XP_011541782.1:n.524+11_524+12dup
XM_011543481.2:c.524+11_524+12dup XP_011541783.1:n.524+11_524+12dup
XM_011543484.2:c.524+11_524+12dup XP_011541786.1:n.524+11_524+12dup
XM_011543485.2:c.524+11_524+12dup XP_011541787.1:n.524+11_524+12dup
XM_011543486.3:c.524+11_524+12dup XP_011541788.1:n.524+11_524+12dup
XM_017009581.1:c.524+11_524+12dup XP_016865070.1:n.524+11_524+12dup
XM_017009583.2:c.-519+11_-519+12dup XP_016865072.1:n.-519+11_-519+12dup
XM_024446113.1:c.524+11_524+12dup XP_024301881.1:n.524+11_524+12dup
XR_001742119.2:n.817+11_817+12dup
NM_001040458.3:c.524+11_524+12dup MANE Select NP_001035548.1:n.524+11_524+12dup
NM_001198541.3:c.524+11_524+12dup NP_001185470.1:n.524+11_524+12dup
NM_001349244.2:c.524+11_524+12dup NP_001336173.1:n.524+11_524+12dup
NM_016442.5:c.524+11_524+12dup NP_057526.3:n.524+11_524+12dup