Canonical Allele Identifier: CA2674689923

Gene: ERAP2 ERAP1

Linked Data

• gnomAD v4: 5-96899980-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96899981_96899982del , CM000667.2:g.96899981_96899982del	GRCh38
NC_000005.9:g.96235685_96235686del , CM000667.1:g.96235685_96235686del	GRCh37
NC_000005.8:g.96261441_96261442del	NCBI36
NG_027839.2:g.41002_41003del
NG_051092.1:g.29043_29044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-140_1504-139del (ERAP2)	ENSP00000421175.2:n.1504-140_1504-139del
ENST00000437043.8:c.1504-140_1504-139del (ERAP2) MANE Select	ENSP00000400376.3:n.1504-140_1504-139del
ENST00000379904.8:c.1369-140_1369-139del (ERAP2)	ENSP00000369235.4:n.1369-140_1369-139del
ENST00000437043.7:c.1504-140_1504-139del (ERAP2)	ENSP00000400376.3:n.1504-140_1504-139del
ENST00000510373.5:c.1504-140_1504-139del (ERAP2)	ENSP00000421175.1:n.1504-140_1504-139del
ENST00000513084.5:c.1504-140_1504-139del (ERAP2)	ENSP00000421849.1:n.1504-140_1504-139del
ENST00000513368.1:n.293-140_293-139del (ERAP2)
ENST00000515095.5:n.415-140_415-139del (ERAP2)
ENST00000515387.1:n.235-140_235-139del (ERAP2)
NM_001130140.1:c.1504-140_1504-139del (ERAP2)	NP_001123612.1:n.1504-140_1504-139del
NM_022350.3:c.1504-140_1504-139del (ERAP2)	NP_071745.1:n.1504-140_1504-139del
XM_011543480.1:c.-705-26310_-705-26309del (ERAP1)	XP_011541782.1:n.-705-26310_-705-26309del
XM_011543481.1:c.-702-26310_-702-26309del (ERAP1)	XP_011541783.1:n.-702-26310_-702-26309del
XM_011543482.1:c.-709-26310_-709-26309del (ERAP1)	XP_011541784.1:n.-709-26310_-709-26309del
XM_011543483.1:c.-872-26310_-872-26309del (ERAP1)	XP_011541785.1:n.-872-26310_-872-26309del
XM_011543484.1:c.-701-26310_-701-26309del (ERAP1)	XP_011541786.1:n.-701-26310_-701-26309del
XM_011543485.1:c.-521-26310_-521-26309del (ERAP1)	XP_011541787.1:n.-521-26310_-521-26309del
XM_011543486.1:c.-705-26310_-705-26309del (ERAP1)	XP_011541788.1:n.-705-26310_-705-26309del
XM_011543487.1:c.-705-26310_-705-26309del (ERAP1)	XP_011541789.1:n.-705-26310_-705-26309del
XM_011543544.1:c.1504-1525_1504-1524del (ERAP2)	XP_011541846.1:n.1504-1525_1504-1524del
XR_948283.1:n.1687-140_1687-139del (ERAP2)
NM_001130140.2:c.1504-140_1504-139del (ERAP2)	NP_001123612.1:n.1504-140_1504-139del
NM_001329229.1:c.1369-140_1369-139del (ERAP2)	NP_001316158.1:n.1369-140_1369-139del
NM_022350.4:c.1504-140_1504-139del (ERAP2)	NP_071745.1:n.1504-140_1504-139del
NR_137637.1:n.2215-140_2215-139del (ERAP2)
XM_011543480.2:c.-705-26310_-705-26309del (ERAP1)	XP_011541782.1:n.-705-26310_-705-26309del
XM_011543481.2:c.-702-26310_-702-26309del (ERAP1)	XP_011541783.1:n.-702-26310_-702-26309del
XM_011543484.2:c.-701-26310_-701-26309del (ERAP1)	XP_011541786.1:n.-701-26310_-701-26309del
XM_011543485.2:c.-521-26310_-521-26309del (ERAP1)	XP_011541787.1:n.-521-26310_-521-26309del
XM_011543486.3:c.-705-26310_-705-26309del (ERAP1)	XP_011541788.1:n.-705-26310_-705-26309del
XM_011543544.2:c.1504-1525_1504-1524del (ERAP2)	XP_011541846.1:n.1504-1525_1504-1524del
XM_017009581.1:c.-547-26604_-547-26603del (ERAP1)	XP_016865070.1:n.-547-26604_-547-26603del
XM_024446113.1:c.-544-26604_-544-26603del (ERAP1)	XP_024301881.1:n.-544-26604_-544-26603del
XR_001742179.2:n.1672-140_1672-139del (ERAP2)
NM_022350.5:c.1504-140_1504-139del (ERAP2) MANE Select	NP_071745.1:n.1504-140_1504-139del