Canonical Allele Identifier: CA1565630409

Gene: ERAP2 ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96899924_96899928delinsCAAAG , CM000667.2:g.96899924_96899928delinsCAAAG	GRCh38
NC_000005.9:g.96235628_96235632delinsCAAAG , CM000667.1:g.96235628_96235632delinsCAAAG	GRCh37
NC_000005.8:g.96261384_96261388delinsCAAAG	NCBI36
NG_027839.2:g.41056_41060delinsCTTTG
NG_051092.1:g.28986_28990delinsCAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1504-197_1504-193delinsCAAAG (ERAP2)	ENSP00000421175.2:n.1504-197_1504-193delinsCAAAG
ENST00000437043.8:c.1504-197_1504-193delinsCAAAG (ERAP2) MANE Select	ENSP00000400376.3:n.1504-197_1504-193delinsCAAAG
ENST00000379904.8:c.1369-197_1369-193delinsCAAAG (ERAP2)	ENSP00000369235.4:n.1369-197_1369-193delinsCAAAG
ENST00000437043.7:c.1504-197_1504-193delinsCAAAG (ERAP2)	ENSP00000400376.3:n.1504-197_1504-193delinsCAAAG
ENST00000510373.5:c.1504-197_1504-193delinsCAAAG (ERAP2)	ENSP00000421175.1:n.1504-197_1504-193delinsCAAAG
ENST00000513084.5:c.1504-197_1504-193delinsCAAAG (ERAP2)	ENSP00000421849.1:n.1504-197_1504-193delinsCAAAG
ENST00000513368.1:n.293-197_293-193delinsCAAAG (ERAP2)
ENST00000515095.5:n.415-197_415-193delinsCAAAG (ERAP2)
ENST00000515387.1:n.235-197_235-193delinsCAAAG (ERAP2)
NM_001130140.1:c.1504-197_1504-193delinsCAAAG (ERAP2)	NP_001123612.1:n.1504-197_1504-193delinsCAAAG
NM_022350.3:c.1504-197_1504-193delinsCAAAG (ERAP2)	NP_071745.1:n.1504-197_1504-193delinsCAAAG
XM_011543480.1:c.-705-26256_-705-26252delinsCTTTG (ERAP1)	XP_011541782.1:n.-705-26256_-705-26252delinsCTTTG
XM_011543481.1:c.-702-26256_-702-26252delinsCTTTG (ERAP1)	XP_011541783.1:n.-702-26256_-702-26252delinsCTTTG
XM_011543482.1:c.-709-26256_-709-26252delinsCTTTG (ERAP1)	XP_011541784.1:n.-709-26256_-709-26252delinsCTTTG
XM_011543483.1:c.-872-26256_-872-26252delinsCTTTG (ERAP1)	XP_011541785.1:n.-872-26256_-872-26252delinsCTTTG
XM_011543484.1:c.-701-26256_-701-26252delinsCTTTG (ERAP1)	XP_011541786.1:n.-701-26256_-701-26252delinsCTTTG
XM_011543485.1:c.-521-26256_-521-26252delinsCTTTG (ERAP1)	XP_011541787.1:n.-521-26256_-521-26252delinsCTTTG
XM_011543486.1:c.-705-26256_-705-26252delinsCTTTG (ERAP1)	XP_011541788.1:n.-705-26256_-705-26252delinsCTTTG
XM_011543487.1:c.-705-26256_-705-26252delinsCTTTG (ERAP1)	XP_011541789.1:n.-705-26256_-705-26252delinsCTTTG
XM_011543544.1:c.1504-1582_1504-1578delinsCAAAG (ERAP2)	XP_011541846.1:n.1504-1582_1504-1578delinsCAAAG
XR_948283.1:n.1687-197_1687-193delinsCAAAG (ERAP2)
NM_001130140.2:c.1504-197_1504-193delinsCAAAG (ERAP2)	NP_001123612.1:n.1504-197_1504-193delinsCAAAG
NM_001329229.1:c.1369-197_1369-193delinsCAAAG (ERAP2)	NP_001316158.1:n.1369-197_1369-193delinsCAAAG
NM_022350.4:c.1504-197_1504-193delinsCAAAG (ERAP2)	NP_071745.1:n.1504-197_1504-193delinsCAAAG
NR_137637.1:n.2215-197_2215-193delinsCAAAG (ERAP2)
XM_011543480.2:c.-705-26256_-705-26252delinsCTTTG (ERAP1)	XP_011541782.1:n.-705-26256_-705-26252delinsCTTTG
XM_011543481.2:c.-702-26256_-702-26252delinsCTTTG (ERAP1)	XP_011541783.1:n.-702-26256_-702-26252delinsCTTTG
XM_011543484.2:c.-701-26256_-701-26252delinsCTTTG (ERAP1)	XP_011541786.1:n.-701-26256_-701-26252delinsCTTTG
XM_011543485.2:c.-521-26256_-521-26252delinsCTTTG (ERAP1)	XP_011541787.1:n.-521-26256_-521-26252delinsCTTTG
XM_011543486.3:c.-705-26256_-705-26252delinsCTTTG (ERAP1)	XP_011541788.1:n.-705-26256_-705-26252delinsCTTTG
XM_011543544.2:c.1504-1582_1504-1578delinsCAAAG (ERAP2)	XP_011541846.1:n.1504-1582_1504-1578delinsCAAAG
XM_017009581.1:c.-547-26550_-547-26546delinsCTTTG (ERAP1)	XP_016865070.1:n.-547-26550_-547-26546delinsCTTTG
XM_024446113.1:c.-544-26550_-544-26546delinsCTTTG (ERAP1)	XP_024301881.1:n.-544-26550_-544-26546delinsCTTTG
XR_001742179.2:n.1672-197_1672-193delinsCAAAG (ERAP2)
NM_022350.5:c.1504-197_1504-193delinsCAAAG (ERAP2) MANE Select	NP_071745.1:n.1504-197_1504-193delinsCAAAG