Canonical Allele Identifier: CA1565580925

Gene: ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96786472_96786473delinsGT , CM000667.2:g.96786472_96786473delinsGT	GRCh38
NC_000005.9:g.96122176_96122177delinsGT , CM000667.1:g.96122176_96122177delinsGT	GRCh37
NC_000005.8:g.96147932_96147933delinsGT	NCBI36
NG_027839.1:g.32672_32673delinsAC
NG_027839.2:g.154511_154512delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.1756_1757delinsAC MANE Select	ENSP00000406304.2:p.Thr586=
ENST00000296754.7:c.1756_1757delinsAC	ENSP00000296754.3:p.Thr586=
ENST00000443439.6:c.1756_1757delinsAC	ENSP00000406304.2:p.Thr586=
ENST00000507859.1:n.419_420delinsAC
ENST00000514604.5:n.180_181delinsAC
NM_001040458.1:c.1756_1757delinsAC	NP_001035548.1:p.Thr586=
NM_001198541.1:c.1756_1757delinsAC	NP_001185470.1:p.Thr586=
NM_016442.3:c.1756_1757delinsAC	NP_057526.3:p.Thr586=
XM_005272015.3:c.1756_1757delinsAC	XP_005272072.1:p.Thr586=
XM_005272016.3:c.1756_1757delinsAC	XP_005272073.1:p.Thr586=
XM_011543480.1:c.1756_1757delinsAC	XP_011541782.1:p.Thr586=
XM_011543481.1:c.1756_1757delinsAC	XP_011541783.1:p.Thr586=
XM_011543482.1:c.1756_1757delinsAC	XP_011541784.1:p.Thr586=
XM_011543483.1:c.1756_1757delinsAC	XP_011541785.1:p.Thr586=
XM_011543484.1:c.1756_1757delinsAC	XP_011541786.1:p.Thr586=
XM_011543485.1:c.1756_1757delinsAC	XP_011541787.1:p.Thr586=
XM_011543486.1:c.1756_1757delinsAC	XP_011541788.1:p.Thr586=
XM_011543487.1:c.1756_1757delinsAC	XP_011541789.1:p.Thr586=
NM_001040458.2:c.1756_1757delinsAC	NP_001035548.1:p.Thr586=
NM_001198541.2:c.1756_1757delinsAC	NP_001185470.1:p.Thr586=
NM_001349244.1:c.1756_1757delinsAC	NP_001336173.1:p.Thr586=
NM_016442.4:c.1756_1757delinsAC	NP_057526.3:p.Thr586=
XM_005272015.5:c.1756_1757delinsAC	XP_005272072.1:p.Thr586=
XM_005272016.4:c.1756_1757delinsAC	XP_005272073.1:p.Thr586=
XM_011543480.2:c.1756_1757delinsAC	XP_011541782.1:p.Thr586=
XM_011543481.2:c.1756_1757delinsAC	XP_011541783.1:p.Thr586=
XM_011543484.2:c.1756_1757delinsAC	XP_011541786.1:p.Thr586=
XM_011543485.2:c.1756_1757delinsAC	XP_011541787.1:p.Thr586=
XM_011543486.3:c.1756_1757delinsAC	XP_011541788.1:p.Thr586=
XM_017009581.1:c.1756_1757delinsAC	XP_016865070.1:p.Thr586=
XM_017009583.2:c.661_662delinsAC	XP_016865072.1:p.Thr221=
XM_024446113.1:c.1756_1757delinsAC	XP_024301881.1:p.Thr586=
XR_001742119.2:n.1894_1895delinsAC
NM_001040458.3:c.1756_1757delinsAC MANE Select	NP_001035548.1:p.Thr586=
NM_001198541.3:c.1756_1757delinsAC	NP_001185470.1:p.Thr586=
NM_001349244.2:c.1756_1757delinsAC	NP_001336173.1:p.Thr586=
NM_016442.5:c.1756_1757delinsAC	NP_057526.3:p.Thr586=