Canonical Allele Identifier: CA360489210
Gene: ERAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96785896T>G , CM000667.2:g.96785896T>G GRCh38
NC_000005.9:g.96121600T>G , CM000667.1:g.96121600T>G GRCh37
NC_000005.8:g.96147356T>G NCBI36
NG_027839.1:g.33249A>C
NG_027839.2:g.155088A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000443439.7:c.1835A>C MANE Select ENSP00000406304.2:p.Tyr612Ser
ENST00000296754.7:c.1835A>C ENSP00000296754.3:p.Tyr612Ser
ENST00000443439.6:c.1835A>C ENSP00000406304.2:p.Tyr612Ser
ENST00000507859.1:n.498A>C
ENST00000514604.5:n.259A>C
NM_001040458.1:c.1835A>C NP_001035548.1:p.Tyr612Ser
NM_001198541.1:c.1835A>C NP_001185470.1:p.Tyr612Ser
NM_016442.3:c.1835A>C NP_057526.3:p.Tyr612Ser
XM_005272015.3:c.1835A>C XP_005272072.1:p.Tyr612Ser
XM_005272016.3:c.1835A>C XP_005272073.1:p.Tyr612Ser
XM_011543480.1:c.1835A>C XP_011541782.1:p.Tyr612Ser
XM_011543481.1:c.1835A>C XP_011541783.1:p.Tyr612Ser
XM_011543482.1:c.1835A>C XP_011541784.1:p.Tyr612Ser
XM_011543483.1:c.1835A>C XP_011541785.1:p.Tyr612Ser
XM_011543484.1:c.1835A>C XP_011541786.1:p.Tyr612Ser
XM_011543485.1:c.1835A>C XP_011541787.1:p.Tyr612Ser
XM_011543486.1:c.1835A>C XP_011541788.1:p.Tyr612Ser
XM_011543487.1:c.1835A>C XP_011541789.1:p.Tyr612Ser
NM_001040458.2:c.1835A>C NP_001035548.1:p.Tyr612Ser
NM_001198541.2:c.1835A>C NP_001185470.1:p.Tyr612Ser
NM_001349244.1:c.1835A>C NP_001336173.1:p.Tyr612Ser
NM_016442.4:c.1835A>C NP_057526.3:p.Tyr612Ser
XM_005272015.5:c.1835A>C XP_005272072.1:p.Tyr612Ser
XM_005272016.4:c.1835A>C XP_005272073.1:p.Tyr612Ser
XM_011543480.2:c.1835A>C XP_011541782.1:p.Tyr612Ser
XM_011543481.2:c.1835A>C XP_011541783.1:p.Tyr612Ser
XM_011543484.2:c.1835A>C XP_011541786.1:p.Tyr612Ser
XM_011543485.2:c.1835A>C XP_011541787.1:p.Tyr612Ser
XM_011543486.3:c.1835A>C XP_011541788.1:p.Tyr612Ser
XM_017009581.1:c.1835A>C XP_016865070.1:p.Tyr612Ser
XM_017009583.2:c.740A>C XP_016865072.1:p.Tyr247Ser
XM_024446113.1:c.1835A>C XP_024301881.1:p.Tyr612Ser
XR_001742119.2:n.1973A>C
XR_001742445.1:n.3853T>G
XR_001742446.1:n.1616T>G
NM_001040458.3:c.1835A>C MANE Select NP_001035548.1:p.Tyr612Ser
NM_001198541.3:c.1835A>C NP_001185470.1:p.Tyr612Ser
NM_001349244.2:c.1835A>C NP_001336173.1:p.Tyr612Ser
NM_016442.5:c.1835A>C NP_057526.3:p.Tyr612Ser