Canonical Allele Identifier: CA2674684423

Gene: ERAP1

Linked Data

• gnomAD v4: 5-96786093-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96786094_96786095del , CM000667.2:g.96786094_96786095del	GRCh38
NC_000005.9:g.96121798_96121799del , CM000667.1:g.96121798_96121799del	GRCh37
NC_000005.8:g.96147554_96147555del	NCBI36
NG_027839.1:g.33050_33051del
NG_027839.2:g.154889_154890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.1760-124_1760-123del MANE Select	ENSP00000406304.2:n.1760-124_1760-123del
ENST00000296754.7:c.1760-124_1760-123del	ENSP00000296754.3:n.1760-124_1760-123del
ENST00000443439.6:c.1760-124_1760-123del	ENSP00000406304.2:n.1760-124_1760-123del
ENST00000507859.1:n.423-124_423-123del
ENST00000514604.5:n.184-124_184-123del
NM_001040458.1:c.1760-124_1760-123del	NP_001035548.1:n.1760-124_1760-123del
NM_001198541.1:c.1760-124_1760-123del	NP_001185470.1:n.1760-124_1760-123del
NM_016442.3:c.1760-124_1760-123del	NP_057526.3:n.1760-124_1760-123del
XM_005272015.3:c.1760-124_1760-123del	XP_005272072.1:n.1760-124_1760-123del
XM_005272016.3:c.1760-124_1760-123del	XP_005272073.1:n.1760-124_1760-123del
XM_011543480.1:c.1760-124_1760-123del	XP_011541782.1:n.1760-124_1760-123del
XM_011543481.1:c.1760-124_1760-123del	XP_011541783.1:n.1760-124_1760-123del
XM_011543482.1:c.1760-124_1760-123del	XP_011541784.1:n.1760-124_1760-123del
XM_011543483.1:c.1760-124_1760-123del	XP_011541785.1:n.1760-124_1760-123del
XM_011543484.1:c.1760-124_1760-123del	XP_011541786.1:n.1760-124_1760-123del
XM_011543485.1:c.1760-124_1760-123del	XP_011541787.1:n.1760-124_1760-123del
XM_011543486.1:c.1760-124_1760-123del	XP_011541788.1:n.1760-124_1760-123del
XM_011543487.1:c.1760-124_1760-123del	XP_011541789.1:n.1760-124_1760-123del
NM_001040458.2:c.1760-124_1760-123del	NP_001035548.1:n.1760-124_1760-123del
NM_001198541.2:c.1760-124_1760-123del	NP_001185470.1:n.1760-124_1760-123del
NM_001349244.1:c.1760-124_1760-123del	NP_001336173.1:n.1760-124_1760-123del
NM_016442.4:c.1760-124_1760-123del	NP_057526.3:n.1760-124_1760-123del
XM_005272015.5:c.1760-124_1760-123del	XP_005272072.1:n.1760-124_1760-123del
XM_005272016.4:c.1760-124_1760-123del	XP_005272073.1:n.1760-124_1760-123del
XM_011543480.2:c.1760-124_1760-123del	XP_011541782.1:n.1760-124_1760-123del
XM_011543481.2:c.1760-124_1760-123del	XP_011541783.1:n.1760-124_1760-123del
XM_011543484.2:c.1760-124_1760-123del	XP_011541786.1:n.1760-124_1760-123del
XM_011543485.2:c.1760-124_1760-123del	XP_011541787.1:n.1760-124_1760-123del
XM_011543486.3:c.1760-124_1760-123del	XP_011541788.1:n.1760-124_1760-123del
XM_017009581.1:c.1760-124_1760-123del	XP_016865070.1:n.1760-124_1760-123del
XM_017009583.2:c.665-124_665-123del	XP_016865072.1:n.665-124_665-123del
XM_024446113.1:c.1760-124_1760-123del	XP_024301881.1:n.1760-124_1760-123del
XR_001742119.2:n.1898-124_1898-123del
NM_001040458.3:c.1760-124_1760-123del MANE Select	NP_001035548.1:n.1760-124_1760-123del
NM_001198541.3:c.1760-124_1760-123del	NP_001185470.1:n.1760-124_1760-123del
NM_001349244.2:c.1760-124_1760-123del	NP_001336173.1:n.1760-124_1760-123del
NM_016442.5:c.1760-124_1760-123del	NP_057526.3:n.1760-124_1760-123del