Canonical Allele Identifier: CA561295197

Gene: ERAP2 ERAP1

Linked Data

• dbSNP Id: rs1282944590
• gnomAD v2: 5-96235581-CTT-C
• gnomAD v3: 5-96899877-CTT-C
• gnomAD v4: 5-96899877-CTT-C
• MyVariant Identifiers: chr5:g.96235582_96235583del (hg19) ; chr5:g.96899878_96899879del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96899879_96899880del , CM000667.2:g.96899879_96899880del	GRCh38
NC_000005.9:g.96235583_96235584del , CM000667.1:g.96235583_96235584del	GRCh37
NC_000005.8:g.96261339_96261340del	NCBI36
NG_027839.2:g.41105_41106del
NG_051092.1:g.28941_28942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-242_1504-241del (ERAP2)	ENSP00000421175.2:n.1504-242_1504-241del
ENST00000437043.8:c.1504-242_1504-241del (ERAP2) MANE Select	ENSP00000400376.3:n.1504-242_1504-241del
ENST00000379904.8:c.1369-242_1369-241del (ERAP2)	ENSP00000369235.4:n.1369-242_1369-241del
ENST00000437043.7:c.1504-242_1504-241del (ERAP2)	ENSP00000400376.3:n.1504-242_1504-241del
ENST00000510373.5:c.1504-242_1504-241del (ERAP2)	ENSP00000421175.1:n.1504-242_1504-241del
ENST00000513084.5:c.1504-242_1504-241del (ERAP2)	ENSP00000421849.1:n.1504-242_1504-241del
ENST00000513368.1:n.293-242_293-241del (ERAP2)
ENST00000515095.5:n.415-242_415-241del (ERAP2)
ENST00000515387.1:n.235-242_235-241del (ERAP2)
NM_001130140.1:c.1504-242_1504-241del (ERAP2)	NP_001123612.1:n.1504-242_1504-241del
NM_022350.3:c.1504-242_1504-241del (ERAP2)	NP_071745.1:n.1504-242_1504-241del
XM_011543480.1:c.-705-26207_-705-26206del (ERAP1)	XP_011541782.1:n.-705-26207_-705-26206del
XM_011543481.1:c.-702-26207_-702-26206del (ERAP1)	XP_011541783.1:n.-702-26207_-702-26206del
XM_011543482.1:c.-709-26207_-709-26206del (ERAP1)	XP_011541784.1:n.-709-26207_-709-26206del
XM_011543483.1:c.-872-26207_-872-26206del (ERAP1)	XP_011541785.1:n.-872-26207_-872-26206del
XM_011543484.1:c.-701-26207_-701-26206del (ERAP1)	XP_011541786.1:n.-701-26207_-701-26206del
XM_011543485.1:c.-521-26207_-521-26206del (ERAP1)	XP_011541787.1:n.-521-26207_-521-26206del
XM_011543486.1:c.-705-26207_-705-26206del (ERAP1)	XP_011541788.1:n.-705-26207_-705-26206del
XM_011543487.1:c.-705-26207_-705-26206del (ERAP1)	XP_011541789.1:n.-705-26207_-705-26206del
XM_011543544.1:c.1504-1627_1504-1626del (ERAP2)	XP_011541846.1:n.1504-1627_1504-1626del
XR_948283.1:n.1687-242_1687-241del (ERAP2)
NM_001130140.2:c.1504-242_1504-241del (ERAP2)	NP_001123612.1:n.1504-242_1504-241del
NM_001329229.1:c.1369-242_1369-241del (ERAP2)	NP_001316158.1:n.1369-242_1369-241del
NM_022350.4:c.1504-242_1504-241del (ERAP2)	NP_071745.1:n.1504-242_1504-241del
NR_137637.1:n.2215-242_2215-241del (ERAP2)
XM_011543480.2:c.-705-26207_-705-26206del (ERAP1)	XP_011541782.1:n.-705-26207_-705-26206del
XM_011543481.2:c.-702-26207_-702-26206del (ERAP1)	XP_011541783.1:n.-702-26207_-702-26206del
XM_011543484.2:c.-701-26207_-701-26206del (ERAP1)	XP_011541786.1:n.-701-26207_-701-26206del
XM_011543485.2:c.-521-26207_-521-26206del (ERAP1)	XP_011541787.1:n.-521-26207_-521-26206del
XM_011543486.3:c.-705-26207_-705-26206del (ERAP1)	XP_011541788.1:n.-705-26207_-705-26206del
XM_011543544.2:c.1504-1627_1504-1626del (ERAP2)	XP_011541846.1:n.1504-1627_1504-1626del
XM_017009581.1:c.-547-26501_-547-26500del (ERAP1)	XP_016865070.1:n.-547-26501_-547-26500del
XM_024446113.1:c.-544-26501_-544-26500del (ERAP1)	XP_024301881.1:n.-544-26501_-544-26500del
XR_001742179.2:n.1672-242_1672-241del (ERAP2)
NM_022350.5:c.1504-242_1504-241del (ERAP2) MANE Select	NP_071745.1:n.1504-242_1504-241del