Canonical Allele Identifier: CA1565580921
Gene: ERAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96786467T>C , CM000667.2:g.96786467T>C GRCh38
NC_000005.9:g.96122171T>C , CM000667.1:g.96122171T>C GRCh37
NC_000005.8:g.96147927T>C NCBI36
NG_027839.1:g.32678A>G
NG_027839.2:g.154517A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000443439.7:c.1759+3A>G MANE Select ENSP00000406304.2:n.1759+3A>G
ENST00000296754.7:c.1759+3A>G ENSP00000296754.3:n.1759+3A>G
ENST00000443439.6:c.1759+3A>G ENSP00000406304.2:n.1759+3A>G
ENST00000507859.1:n.422+3A>G
ENST00000514604.5:n.183+3A>G
NM_001040458.1:c.1759+3A>G NP_001035548.1:n.1759+3A>G
NM_001198541.1:c.1759+3A>G NP_001185470.1:n.1759+3A>G
NM_016442.3:c.1759+3A>G NP_057526.3:n.1759+3A>G
XM_005272015.3:c.1759+3A>G XP_005272072.1:n.1759+3A>G
XM_005272016.3:c.1759+3A>G XP_005272073.1:n.1759+3A>G
XM_011543480.1:c.1759+3A>G XP_011541782.1:n.1759+3A>G
XM_011543481.1:c.1759+3A>G XP_011541783.1:n.1759+3A>G
XM_011543482.1:c.1759+3A>G XP_011541784.1:n.1759+3A>G
XM_011543483.1:c.1759+3A>G XP_011541785.1:n.1759+3A>G
XM_011543484.1:c.1759+3A>G XP_011541786.1:n.1759+3A>G
XM_011543485.1:c.1759+3A>G XP_011541787.1:n.1759+3A>G
XM_011543486.1:c.1759+3A>G XP_011541788.1:n.1759+3A>G
XM_011543487.1:c.1759+3A>G XP_011541789.1:n.1759+3A>G
NM_001040458.2:c.1759+3A>G NP_001035548.1:n.1759+3A>G
NM_001198541.2:c.1759+3A>G NP_001185470.1:n.1759+3A>G
NM_001349244.1:c.1759+3A>G NP_001336173.1:n.1759+3A>G
NM_016442.4:c.1759+3A>G NP_057526.3:n.1759+3A>G
XM_005272015.5:c.1759+3A>G XP_005272072.1:n.1759+3A>G
XM_005272016.4:c.1759+3A>G XP_005272073.1:n.1759+3A>G
XM_011543480.2:c.1759+3A>G XP_011541782.1:n.1759+3A>G
XM_011543481.2:c.1759+3A>G XP_011541783.1:n.1759+3A>G
XM_011543484.2:c.1759+3A>G XP_011541786.1:n.1759+3A>G
XM_011543485.2:c.1759+3A>G XP_011541787.1:n.1759+3A>G
XM_011543486.3:c.1759+3A>G XP_011541788.1:n.1759+3A>G
XM_017009581.1:c.1759+3A>G XP_016865070.1:n.1759+3A>G
XM_017009583.2:c.664+3A>G XP_016865072.1:n.664+3A>G
XM_024446113.1:c.1759+3A>G XP_024301881.1:n.1759+3A>G
XR_001742119.2:n.1897+3A>G
NM_001040458.3:c.1759+3A>G MANE Select NP_001035548.1:n.1759+3A>G
NM_001198541.3:c.1759+3A>G NP_001185470.1:n.1759+3A>G
NM_001349244.2:c.1759+3A>G NP_001336173.1:n.1759+3A>G
NM_016442.5:c.1759+3A>G NP_057526.3:n.1759+3A>G