Canonical Allele Identifier: CA1565630410

Gene: ERAP2 ERAP1

Linked Data

• dbSNP Id: rs1785270087

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96899928_96899931del , CM000667.2:g.96899928_96899931del	GRCh38
NC_000005.9:g.96235632_96235635del , CM000667.1:g.96235632_96235635del	GRCh37
NC_000005.8:g.96261388_96261391del	NCBI36
NG_027839.2:g.41056_41059del
NG_051092.1:g.28990_28993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-193_1504-190del (ERAP2)	ENSP00000421175.2:n.1504-193_1504-190del
ENST00000437043.8:c.1504-193_1504-190del (ERAP2) MANE Select	ENSP00000400376.3:n.1504-193_1504-190del
ENST00000379904.8:c.1369-193_1369-190del (ERAP2)	ENSP00000369235.4:n.1369-193_1369-190del
ENST00000437043.7:c.1504-193_1504-190del (ERAP2)	ENSP00000400376.3:n.1504-193_1504-190del
ENST00000510373.5:c.1504-193_1504-190del (ERAP2)	ENSP00000421175.1:n.1504-193_1504-190del
ENST00000513084.5:c.1504-193_1504-190del (ERAP2)	ENSP00000421849.1:n.1504-193_1504-190del
ENST00000513368.1:n.293-193_293-190del (ERAP2)
ENST00000515095.5:n.415-193_415-190del (ERAP2)
ENST00000515387.1:n.235-193_235-190del (ERAP2)
NM_001130140.1:c.1504-193_1504-190del (ERAP2)	NP_001123612.1:n.1504-193_1504-190del
NM_022350.3:c.1504-193_1504-190del (ERAP2)	NP_071745.1:n.1504-193_1504-190del
XM_011543480.1:c.-705-26256_-705-26253del (ERAP1)	XP_011541782.1:n.-705-26256_-705-26253del
XM_011543481.1:c.-702-26256_-702-26253del (ERAP1)	XP_011541783.1:n.-702-26256_-702-26253del
XM_011543482.1:c.-709-26256_-709-26253del (ERAP1)	XP_011541784.1:n.-709-26256_-709-26253del
XM_011543483.1:c.-872-26256_-872-26253del (ERAP1)	XP_011541785.1:n.-872-26256_-872-26253del
XM_011543484.1:c.-701-26256_-701-26253del (ERAP1)	XP_011541786.1:n.-701-26256_-701-26253del
XM_011543485.1:c.-521-26256_-521-26253del (ERAP1)	XP_011541787.1:n.-521-26256_-521-26253del
XM_011543486.1:c.-705-26256_-705-26253del (ERAP1)	XP_011541788.1:n.-705-26256_-705-26253del
XM_011543487.1:c.-705-26256_-705-26253del (ERAP1)	XP_011541789.1:n.-705-26256_-705-26253del
XM_011543544.1:c.1504-1578_1504-1575del (ERAP2)	XP_011541846.1:n.1504-1578_1504-1575del
XR_948283.1:n.1687-193_1687-190del (ERAP2)
NM_001130140.2:c.1504-193_1504-190del (ERAP2)	NP_001123612.1:n.1504-193_1504-190del
NM_001329229.1:c.1369-193_1369-190del (ERAP2)	NP_001316158.1:n.1369-193_1369-190del
NM_022350.4:c.1504-193_1504-190del (ERAP2)	NP_071745.1:n.1504-193_1504-190del
NR_137637.1:n.2215-193_2215-190del (ERAP2)
XM_011543480.2:c.-705-26256_-705-26253del (ERAP1)	XP_011541782.1:n.-705-26256_-705-26253del
XM_011543481.2:c.-702-26256_-702-26253del (ERAP1)	XP_011541783.1:n.-702-26256_-702-26253del
XM_011543484.2:c.-701-26256_-701-26253del (ERAP1)	XP_011541786.1:n.-701-26256_-701-26253del
XM_011543485.2:c.-521-26256_-521-26253del (ERAP1)	XP_011541787.1:n.-521-26256_-521-26253del
XM_011543486.3:c.-705-26256_-705-26253del (ERAP1)	XP_011541788.1:n.-705-26256_-705-26253del
XM_011543544.2:c.1504-1578_1504-1575del (ERAP2)	XP_011541846.1:n.1504-1578_1504-1575del
XM_017009581.1:c.-547-26550_-547-26547del (ERAP1)	XP_016865070.1:n.-547-26550_-547-26547del
XM_024446113.1:c.-544-26550_-544-26547del (ERAP1)	XP_024301881.1:n.-544-26550_-544-26547del
XR_001742179.2:n.1672-193_1672-190del (ERAP2)
NM_022350.5:c.1504-193_1504-190del (ERAP2) MANE Select	NP_071745.1:n.1504-193_1504-190del