Canonical Allele Identifier: CA2674683740
Gene: ERAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96785667_96785669dup , CM000667.2:g.96785667_96785669dup GRCh38
NC_000005.9:g.96121371_96121373dup , CM000667.1:g.96121371_96121373dup GRCh37
NC_000005.8:g.96147127_96147129dup NCBI36
NG_027839.1:g.33476_33478dup
NG_027839.2:g.155315_155317dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.1943+119_1943+121dup MANE Select ENSP00000406304.2:n.1943+119_1943+121dup
ENST00000296754.7:c.1943+119_1943+121dup ENSP00000296754.3:n.1943+119_1943+121dup
ENST00000443439.6:c.1943+119_1943+121dup ENSP00000406304.2:n.1943+119_1943+121dup
ENST00000507859.1:n.725_727dup
ENST00000514604.5:n.367+119_367+121dup
NM_001040458.1:c.1943+119_1943+121dup NP_001035548.1:n.1943+119_1943+121dup
NM_001198541.1:c.1943+119_1943+121dup NP_001185470.1:n.1943+119_1943+121dup
NM_016442.3:c.1943+119_1943+121dup NP_057526.3:n.1943+119_1943+121dup
XM_005272015.3:c.1943+119_1943+121dup XP_005272072.1:n.1943+119_1943+121dup
XM_005272016.3:c.1943+119_1943+121dup XP_005272073.1:n.1943+119_1943+121dup
XM_011543480.1:c.1943+119_1943+121dup XP_011541782.1:n.1943+119_1943+121dup
XM_011543481.1:c.1943+119_1943+121dup XP_011541783.1:n.1943+119_1943+121dup
XM_011543482.1:c.1943+119_1943+121dup XP_011541784.1:n.1943+119_1943+121dup
XM_011543483.1:c.1943+119_1943+121dup XP_011541785.1:n.1943+119_1943+121dup
XM_011543484.1:c.1943+119_1943+121dup XP_011541786.1:n.1943+119_1943+121dup
XM_011543485.1:c.1943+119_1943+121dup XP_011541787.1:n.1943+119_1943+121dup
XM_011543486.1:c.1943+119_1943+121dup XP_011541788.1:n.1943+119_1943+121dup
XM_011543487.1:c.1943+119_1943+121dup XP_011541789.1:n.1943+119_1943+121dup
XR_427744.2:n.435_437dup
XR_948592.1:n.751_753dup
XR_948593.1:n.1059_1061dup
XR_948594.1:n.733_735dup
XR_948595.1:n.743_745dup
NM_001040458.2:c.1943+119_1943+121dup NP_001035548.1:n.1943+119_1943+121dup
NM_001198541.2:c.1943+119_1943+121dup NP_001185470.1:n.1943+119_1943+121dup
NM_001349244.1:c.1943+119_1943+121dup NP_001336173.1:n.1943+119_1943+121dup
NM_016442.4:c.1943+119_1943+121dup NP_057526.3:n.1943+119_1943+121dup
XM_005272015.5:c.1943+119_1943+121dup XP_005272072.1:n.1943+119_1943+121dup
XM_005272016.4:c.1943+119_1943+121dup XP_005272073.1:n.1943+119_1943+121dup
XM_011543480.2:c.1943+119_1943+121dup XP_011541782.1:n.1943+119_1943+121dup
XM_011543481.2:c.1943+119_1943+121dup XP_011541783.1:n.1943+119_1943+121dup
XM_011543484.2:c.1943+119_1943+121dup XP_011541786.1:n.1943+119_1943+121dup
XM_011543485.2:c.1943+119_1943+121dup XP_011541787.1:n.1943+119_1943+121dup
XM_011543486.3:c.1943+119_1943+121dup XP_011541788.1:n.1943+119_1943+121dup
XM_017009581.1:c.1943+119_1943+121dup XP_016865070.1:n.1943+119_1943+121dup
XM_017009583.2:c.848+119_848+121dup XP_016865072.1:n.848+119_848+121dup
XM_024446113.1:c.1943+119_1943+121dup XP_024301881.1:n.1943+119_1943+121dup
XR_001742119.2:n.2081+119_2081+121dup
XR_001742445.1:n.3624_3626dup
XR_001742446.1:n.1387_1389dup
NM_001040458.3:c.1943+119_1943+121dup MANE Select NP_001035548.1:n.1943+119_1943+121dup
NM_001198541.3:c.1943+119_1943+121dup NP_001185470.1:n.1943+119_1943+121dup
NM_001349244.2:c.1943+119_1943+121dup NP_001336173.1:n.1943+119_1943+121dup
NM_016442.5:c.1943+119_1943+121dup NP_057526.3:n.1943+119_1943+121dup