Canonical Allele Identifier: CA2842435348

Gene: ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96786106_96786107del , CM000667.2:g.96786106_96786107del	GRCh38
NC_000005.9:g.96121810_96121811del , CM000667.1:g.96121810_96121811del	GRCh37
NC_000005.8:g.96147566_96147567del	NCBI36
NG_027839.1:g.33039_33040del
NG_027839.2:g.154878_154879del

Transcript Alleles

HGVS	Amino-acid Change
NM_001040458.3:c.1760-135_1760-134del MANE Select	NP_001035548.1:n.1760-135_1760-134del
ENST00000443439.7:c.1760-135_1760-134del MANE Select	ENSP00000406304.2:n.1760-135_1760-134del
NM_001040458.1:c.1760-135_1760-134del	NP_001035548.1:n.1760-135_1760-134del
NM_001040458.2:c.1760-135_1760-134del	NP_001035548.1:n.1760-135_1760-134del
NM_001198541.1:c.1760-135_1760-134del	NP_001185470.1:n.1760-135_1760-134del
NM_001198541.2:c.1760-135_1760-134del	NP_001185470.1:n.1760-135_1760-134del
NM_001198541.3:c.1760-135_1760-134del	NP_001185470.1:n.1760-135_1760-134del
NM_001349244.1:c.1760-135_1760-134del	NP_001336173.1:n.1760-135_1760-134del
NM_001349244.2:c.1760-135_1760-134del	NP_001336173.1:n.1760-135_1760-134del
NM_016442.3:c.1760-135_1760-134del	NP_057526.3:n.1760-135_1760-134del
NM_016442.4:c.1760-135_1760-134del	NP_057526.3:n.1760-135_1760-134del
NM_016442.5:c.1760-135_1760-134del	NP_057526.3:n.1760-135_1760-134del
ENST00000296754.7:c.1760-135_1760-134del	ENSP00000296754.3:n.1760-135_1760-134del
ENST00000443439.6:c.1760-135_1760-134del	ENSP00000406304.2:n.1760-135_1760-134del
ENST00000507859.1:n.423-135_423-134del
ENST00000514604.5:n.184-135_184-134del
XM_005272015.3:c.1760-135_1760-134del	XP_005272072.1:n.1760-135_1760-134del
XM_005272015.5:c.1760-135_1760-134del	XP_005272072.1:n.1760-135_1760-134del
XM_005272016.3:c.1760-135_1760-134del	XP_005272073.1:n.1760-135_1760-134del
XM_005272016.4:c.1760-135_1760-134del	XP_005272073.1:n.1760-135_1760-134del
XM_011543480.1:c.1760-135_1760-134del	XP_011541782.1:n.1760-135_1760-134del
XM_011543480.2:c.1760-135_1760-134del	XP_011541782.1:n.1760-135_1760-134del
XM_011543481.1:c.1760-135_1760-134del	XP_011541783.1:n.1760-135_1760-134del
XM_011543481.2:c.1760-135_1760-134del	XP_011541783.1:n.1760-135_1760-134del
XM_011543482.1:c.1760-135_1760-134del	XP_011541784.1:n.1760-135_1760-134del
XM_011543483.1:c.1760-135_1760-134del	XP_011541785.1:n.1760-135_1760-134del
XM_011543484.1:c.1760-135_1760-134del	XP_011541786.1:n.1760-135_1760-134del
XM_011543484.2:c.1760-135_1760-134del	XP_011541786.1:n.1760-135_1760-134del
XM_011543485.1:c.1760-135_1760-134del	XP_011541787.1:n.1760-135_1760-134del
XM_011543485.2:c.1760-135_1760-134del	XP_011541787.1:n.1760-135_1760-134del
XM_011543486.1:c.1760-135_1760-134del	XP_011541788.1:n.1760-135_1760-134del
XM_011543486.3:c.1760-135_1760-134del	XP_011541788.1:n.1760-135_1760-134del
XM_011543487.1:c.1760-135_1760-134del	XP_011541789.1:n.1760-135_1760-134del
XM_017009581.1:c.1760-135_1760-134del	XP_016865070.1:n.1760-135_1760-134del
XM_017009583.2:c.665-135_665-134del	XP_016865072.1:n.665-135_665-134del
XM_024446113.1:c.1760-135_1760-134del	XP_024301881.1:n.1760-135_1760-134del
XR_001742119.2:n.1898-135_1898-134del