Canonical Allele Identifier: CA2674689931

Gene: ERAP2 ERAP1

Linked Data

• gnomAD v4: 5-96899991-GTTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96899994_96899997del , CM000667.2:g.96899994_96899997del	GRCh38
NC_000005.9:g.96235698_96235701del , CM000667.1:g.96235698_96235701del	GRCh37
NC_000005.8:g.96261454_96261457del	NCBI36
NG_027839.2:g.40989_40992del
NG_051092.1:g.29056_29059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-127_1504-124del (ERAP2)	ENSP00000421175.2:n.1504-127_1504-124del
ENST00000437043.8:c.1504-127_1504-124del (ERAP2) MANE Select	ENSP00000400376.3:n.1504-127_1504-124del
ENST00000379904.8:c.1369-127_1369-124del (ERAP2)	ENSP00000369235.4:n.1369-127_1369-124del
ENST00000437043.7:c.1504-127_1504-124del (ERAP2)	ENSP00000400376.3:n.1504-127_1504-124del
ENST00000510373.5:c.1504-127_1504-124del (ERAP2)	ENSP00000421175.1:n.1504-127_1504-124del
ENST00000513084.5:c.1504-127_1504-124del (ERAP2)	ENSP00000421849.1:n.1504-127_1504-124del
ENST00000513368.1:n.293-127_293-124del (ERAP2)
ENST00000515095.5:n.415-127_415-124del (ERAP2)
ENST00000515387.1:n.235-127_235-124del (ERAP2)
NM_001130140.1:c.1504-127_1504-124del (ERAP2)	NP_001123612.1:n.1504-127_1504-124del
NM_022350.3:c.1504-127_1504-124del (ERAP2)	NP_071745.1:n.1504-127_1504-124del
XM_011543480.1:c.-705-26323_-705-26320del (ERAP1)	XP_011541782.1:n.-705-26323_-705-26320del
XM_011543481.1:c.-702-26323_-702-26320del (ERAP1)	XP_011541783.1:n.-702-26323_-702-26320del
XM_011543482.1:c.-709-26323_-709-26320del (ERAP1)	XP_011541784.1:n.-709-26323_-709-26320del
XM_011543483.1:c.-872-26323_-872-26320del (ERAP1)	XP_011541785.1:n.-872-26323_-872-26320del
XM_011543484.1:c.-701-26323_-701-26320del (ERAP1)	XP_011541786.1:n.-701-26323_-701-26320del
XM_011543485.1:c.-521-26323_-521-26320del (ERAP1)	XP_011541787.1:n.-521-26323_-521-26320del
XM_011543486.1:c.-705-26323_-705-26320del (ERAP1)	XP_011541788.1:n.-705-26323_-705-26320del
XM_011543487.1:c.-705-26323_-705-26320del (ERAP1)	XP_011541789.1:n.-705-26323_-705-26320del
XM_011543544.1:c.1504-1512_1504-1509del (ERAP2)	XP_011541846.1:n.1504-1512_1504-1509del
XR_948283.1:n.1687-127_1687-124del (ERAP2)
NM_001130140.2:c.1504-127_1504-124del (ERAP2)	NP_001123612.1:n.1504-127_1504-124del
NM_001329229.1:c.1369-127_1369-124del (ERAP2)	NP_001316158.1:n.1369-127_1369-124del
NM_022350.4:c.1504-127_1504-124del (ERAP2)	NP_071745.1:n.1504-127_1504-124del
NR_137637.1:n.2215-127_2215-124del (ERAP2)
XM_011543480.2:c.-705-26323_-705-26320del (ERAP1)	XP_011541782.1:n.-705-26323_-705-26320del
XM_011543481.2:c.-702-26323_-702-26320del (ERAP1)	XP_011541783.1:n.-702-26323_-702-26320del
XM_011543484.2:c.-701-26323_-701-26320del (ERAP1)	XP_011541786.1:n.-701-26323_-701-26320del
XM_011543485.2:c.-521-26323_-521-26320del (ERAP1)	XP_011541787.1:n.-521-26323_-521-26320del
XM_011543486.3:c.-705-26323_-705-26320del (ERAP1)	XP_011541788.1:n.-705-26323_-705-26320del
XM_011543544.2:c.1504-1512_1504-1509del (ERAP2)	XP_011541846.1:n.1504-1512_1504-1509del
XM_017009581.1:c.-547-26617_-547-26614del (ERAP1)	XP_016865070.1:n.-547-26617_-547-26614del
XM_024446113.1:c.-544-26617_-544-26614del (ERAP1)	XP_024301881.1:n.-544-26617_-544-26614del
XR_001742179.2:n.1672-127_1672-124del (ERAP2)
NM_022350.5:c.1504-127_1504-124del (ERAP2) MANE Select	NP_071745.1:n.1504-127_1504-124del