Canonical Allele Identifier: CA1565580640
Gene: ERAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96785733_96785736delinsGAAC , CM000667.2:g.96785733_96785736delinsGAAC GRCh38
NC_000005.9:g.96121437_96121440delinsGAAC , CM000667.1:g.96121437_96121440delinsGAAC GRCh37
NC_000005.8:g.96147193_96147196delinsGAAC NCBI36
NG_027839.1:g.33409_33412delinsGTTC
NG_027839.2:g.155248_155251delinsGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.1943+52_1943+55delinsGTTC MANE Select ENSP00000406304.2:n.1943+52_1943+55delinsGTTC
ENST00000296754.7:c.1943+52_1943+55delinsGTTC ENSP00000296754.3:n.1943+52_1943+55delinsGTTC
ENST00000443439.6:c.1943+52_1943+55delinsGTTC ENSP00000406304.2:n.1943+52_1943+55delinsGTTC
ENST00000507859.1:n.658_661delinsGTTC
ENST00000514604.5:n.367+52_367+55delinsGTTC
NM_001040458.1:c.1943+52_1943+55delinsGTTC NP_001035548.1:n.1943+52_1943+55delinsGTTC
NM_001198541.1:c.1943+52_1943+55delinsGTTC NP_001185470.1:n.1943+52_1943+55delinsGTTC
NM_016442.3:c.1943+52_1943+55delinsGTTC NP_057526.3:n.1943+52_1943+55delinsGTTC
XM_005272015.3:c.1943+52_1943+55delinsGTTC XP_005272072.1:n.1943+52_1943+55delinsGTTC
XM_005272016.3:c.1943+52_1943+55delinsGTTC XP_005272073.1:n.1943+52_1943+55delinsGTTC
XM_011543480.1:c.1943+52_1943+55delinsGTTC XP_011541782.1:n.1943+52_1943+55delinsGTTC
XM_011543481.1:c.1943+52_1943+55delinsGTTC XP_011541783.1:n.1943+52_1943+55delinsGTTC
XM_011543482.1:c.1943+52_1943+55delinsGTTC XP_011541784.1:n.1943+52_1943+55delinsGTTC
XM_011543483.1:c.1943+52_1943+55delinsGTTC XP_011541785.1:n.1943+52_1943+55delinsGTTC
XM_011543484.1:c.1943+52_1943+55delinsGTTC XP_011541786.1:n.1943+52_1943+55delinsGTTC
XM_011543485.1:c.1943+52_1943+55delinsGTTC XP_011541787.1:n.1943+52_1943+55delinsGTTC
XM_011543486.1:c.1943+52_1943+55delinsGTTC XP_011541788.1:n.1943+52_1943+55delinsGTTC
XM_011543487.1:c.1943+52_1943+55delinsGTTC XP_011541789.1:n.1943+52_1943+55delinsGTTC
XR_427744.2:n.501_504delinsGAAC
XR_948592.1:n.817_820delinsGAAC
XR_948593.1:n.1125_1128delinsGAAC
XR_948594.1:n.799_802delinsGAAC
XR_948595.1:n.809_812delinsGAAC
NM_001040458.2:c.1943+52_1943+55delinsGTTC NP_001035548.1:n.1943+52_1943+55delinsGTTC
NM_001198541.2:c.1943+52_1943+55delinsGTTC NP_001185470.1:n.1943+52_1943+55delinsGTTC
NM_001349244.1:c.1943+52_1943+55delinsGTTC NP_001336173.1:n.1943+52_1943+55delinsGTTC
NM_016442.4:c.1943+52_1943+55delinsGTTC NP_057526.3:n.1943+52_1943+55delinsGTTC
XM_005272015.5:c.1943+52_1943+55delinsGTTC XP_005272072.1:n.1943+52_1943+55delinsGTTC
XM_005272016.4:c.1943+52_1943+55delinsGTTC XP_005272073.1:n.1943+52_1943+55delinsGTTC
XM_011543480.2:c.1943+52_1943+55delinsGTTC XP_011541782.1:n.1943+52_1943+55delinsGTTC
XM_011543481.2:c.1943+52_1943+55delinsGTTC XP_011541783.1:n.1943+52_1943+55delinsGTTC
XM_011543484.2:c.1943+52_1943+55delinsGTTC XP_011541786.1:n.1943+52_1943+55delinsGTTC
XM_011543485.2:c.1943+52_1943+55delinsGTTC XP_011541787.1:n.1943+52_1943+55delinsGTTC
XM_011543486.3:c.1943+52_1943+55delinsGTTC XP_011541788.1:n.1943+52_1943+55delinsGTTC
XM_017009581.1:c.1943+52_1943+55delinsGTTC XP_016865070.1:n.1943+52_1943+55delinsGTTC
XM_017009583.2:c.848+52_848+55delinsGTTC XP_016865072.1:n.848+52_848+55delinsGTTC
XM_024446113.1:c.1943+52_1943+55delinsGTTC XP_024301881.1:n.1943+52_1943+55delinsGTTC
XR_001742119.2:n.2081+52_2081+55delinsGTTC
XR_001742445.1:n.3690_3693delinsGAAC
XR_001742446.1:n.1453_1456delinsGAAC
NM_001040458.3:c.1943+52_1943+55delinsGTTC MANE Select NP_001035548.1:n.1943+52_1943+55delinsGTTC
NM_001198541.3:c.1943+52_1943+55delinsGTTC NP_001185470.1:n.1943+52_1943+55delinsGTTC
NM_001349244.2:c.1943+52_1943+55delinsGTTC NP_001336173.1:n.1943+52_1943+55delinsGTTC
NM_016442.5:c.1943+52_1943+55delinsGTTC NP_057526.3:n.1943+52_1943+55delinsGTTC