Canonical Allele Identifier: CA1565630477

Gene: ERAP2 ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96900071_96900085delinsGCCAACTAATGATGC , CM000667.2:g.96900071_96900085delinsGCCAACTAATGATGC	GRCh38
NC_000005.9:g.96235775_96235789delinsGCCAACTAATGATGC , CM000667.1:g.96235775_96235789delinsGCCAACTAATGATGC	GRCh37
NC_000005.8:g.96261531_96261545delinsGCCAACTAATGATGC	NCBI36
NG_027839.2:g.40899_40913delinsGCATCATTAGTTGGC
NG_051092.1:g.29133_29147delinsGCCAACTAATGATGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	ENSP00000421175.2:n.1504-50_1504-36delinsGCCAACTAATGATGC
ENST00000437043.8:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2) MANE Select	ENSP00000400376.3:n.1504-50_1504-36delinsGCCAACTAATGATGC
ENST00000379904.8:c.1369-50_1369-36delinsGCCAACTAATGATGC (ERAP2)	ENSP00000369235.4:n.1369-50_1369-36delinsGCCAACTAATGATGC
ENST00000437043.7:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	ENSP00000400376.3:n.1504-50_1504-36delinsGCCAACTAATGATGC
ENST00000510373.5:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	ENSP00000421175.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
ENST00000513084.5:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	ENSP00000421849.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
ENST00000513368.1:n.293-50_293-36delinsGCCAACTAATGATGC (ERAP2)
ENST00000515095.5:n.415-50_415-36delinsGCCAACTAATGATGC (ERAP2)
ENST00000515387.1:n.235-50_235-36delinsGCCAACTAATGATGC (ERAP2)
NM_001130140.1:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	NP_001123612.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
NM_022350.3:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	NP_071745.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
XM_011543480.1:c.-705-26413_-705-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541782.1:n.-705-26413_-705-26399delinsGCATCATTAGTTGGC
XM_011543481.1:c.-702-26413_-702-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541783.1:n.-702-26413_-702-26399delinsGCATCATTAGTTGGC
XM_011543482.1:c.-709-26413_-709-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541784.1:n.-709-26413_-709-26399delinsGCATCATTAGTTGGC
XM_011543483.1:c.-872-26413_-872-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541785.1:n.-872-26413_-872-26399delinsGCATCATTAGTTGGC
XM_011543484.1:c.-701-26413_-701-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541786.1:n.-701-26413_-701-26399delinsGCATCATTAGTTGGC
XM_011543485.1:c.-521-26413_-521-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541787.1:n.-521-26413_-521-26399delinsGCATCATTAGTTGGC
XM_011543486.1:c.-705-26413_-705-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541788.1:n.-705-26413_-705-26399delinsGCATCATTAGTTGGC
XM_011543487.1:c.-705-26413_-705-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541789.1:n.-705-26413_-705-26399delinsGCATCATTAGTTGGC
XM_011543544.1:c.1504-1435_1504-1421delinsGCCAACTAATGATGC (ERAP2)	XP_011541846.1:n.1504-1435_1504-1421delinsGCCAACTAATGATGC
XR_948283.1:n.1687-50_1687-36delinsGCCAACTAATGATGC (ERAP2)
NM_001130140.2:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	NP_001123612.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
NM_001329229.1:c.1369-50_1369-36delinsGCCAACTAATGATGC (ERAP2)	NP_001316158.1:n.1369-50_1369-36delinsGCCAACTAATGATGC
NM_022350.4:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2)	NP_071745.1:n.1504-50_1504-36delinsGCCAACTAATGATGC
NR_137637.1:n.2215-50_2215-36delinsGCCAACTAATGATGC (ERAP2)
XM_011543480.2:c.-705-26413_-705-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541782.1:n.-705-26413_-705-26399delinsGCATCATTAGTTGGC
XM_011543481.2:c.-702-26413_-702-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541783.1:n.-702-26413_-702-26399delinsGCATCATTAGTTGGC
XM_011543484.2:c.-701-26413_-701-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541786.1:n.-701-26413_-701-26399delinsGCATCATTAGTTGGC
XM_011543485.2:c.-521-26413_-521-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541787.1:n.-521-26413_-521-26399delinsGCATCATTAGTTGGC
XM_011543486.3:c.-705-26413_-705-26399delinsGCATCATTAGTTGGC (ERAP1)	XP_011541788.1:n.-705-26413_-705-26399delinsGCATCATTAGTTGGC
XM_011543544.2:c.1504-1435_1504-1421delinsGCCAACTAATGATGC (ERAP2)	XP_011541846.1:n.1504-1435_1504-1421delinsGCCAACTAATGATGC
XM_017009581.1:c.-547-26707_-547-26693delinsGCATCATTAGTTGGC (ERAP1)	XP_016865070.1:n.-547-26707_-547-26693delinsGCATCATTAGTTGGC
XM_024446113.1:c.-544-26707_-544-26693delinsGCATCATTAGTTGGC (ERAP1)	XP_024301881.1:n.-544-26707_-544-26693delinsGCATCATTAGTTGGC
XR_001742179.2:n.1672-50_1672-36delinsGCCAACTAATGATGC (ERAP2)
NM_022350.5:c.1504-50_1504-36delinsGCCAACTAATGATGC (ERAP2) MANE Select	NP_071745.1:n.1504-50_1504-36delinsGCCAACTAATGATGC