Canonical Allele Identifier: CA2674683713

Gene: ERAP1

Linked Data

• gnomAD v4: 5-96785646-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96785647_96785648del , CM000667.2:g.96785647_96785648del	GRCh38
NC_000005.9:g.96121351_96121352del , CM000667.1:g.96121351_96121352del	GRCh37
NC_000005.8:g.96147107_96147108del	NCBI36
NG_027839.1:g.33497_33498del
NG_027839.2:g.155336_155337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.1943+140_1943+141del MANE Select	ENSP00000406304.2:n.1943+140_1943+141del
ENST00000296754.7:c.1943+140_1943+141del	ENSP00000296754.3:n.1943+140_1943+141del
ENST00000443439.6:c.1943+140_1943+141del	ENSP00000406304.2:n.1943+140_1943+141del
ENST00000507859.1:n.746_747del
ENST00000514604.5:n.367+140_367+141del
NM_001040458.1:c.1943+140_1943+141del	NP_001035548.1:n.1943+140_1943+141del
NM_001198541.1:c.1943+140_1943+141del	NP_001185470.1:n.1943+140_1943+141del
NM_016442.3:c.1943+140_1943+141del	NP_057526.3:n.1943+140_1943+141del
XM_005272015.3:c.1943+140_1943+141del	XP_005272072.1:n.1943+140_1943+141del
XM_005272016.3:c.1943+140_1943+141del	XP_005272073.1:n.1943+140_1943+141del
XM_011543480.1:c.1943+140_1943+141del	XP_011541782.1:n.1943+140_1943+141del
XM_011543481.1:c.1943+140_1943+141del	XP_011541783.1:n.1943+140_1943+141del
XM_011543482.1:c.1943+140_1943+141del	XP_011541784.1:n.1943+140_1943+141del
XM_011543483.1:c.1943+140_1943+141del	XP_011541785.1:n.1943+140_1943+141del
XM_011543484.1:c.1943+140_1943+141del	XP_011541786.1:n.1943+140_1943+141del
XM_011543485.1:c.1943+140_1943+141del	XP_011541787.1:n.1943+140_1943+141del
XM_011543486.1:c.1943+140_1943+141del	XP_011541788.1:n.1943+140_1943+141del
XM_011543487.1:c.1943+140_1943+141del	XP_011541789.1:n.1943+140_1943+141del
XR_427744.2:n.415_416del
XR_948592.1:n.731_732del
XR_948593.1:n.1039_1040del
XR_948594.1:n.713_714del
XR_948595.1:n.723_724del
NM_001040458.2:c.1943+140_1943+141del	NP_001035548.1:n.1943+140_1943+141del
NM_001198541.2:c.1943+140_1943+141del	NP_001185470.1:n.1943+140_1943+141del
NM_001349244.1:c.1943+140_1943+141del	NP_001336173.1:n.1943+140_1943+141del
NM_016442.4:c.1943+140_1943+141del	NP_057526.3:n.1943+140_1943+141del
XM_005272015.5:c.1943+140_1943+141del	XP_005272072.1:n.1943+140_1943+141del
XM_005272016.4:c.1943+140_1943+141del	XP_005272073.1:n.1943+140_1943+141del
XM_011543480.2:c.1943+140_1943+141del	XP_011541782.1:n.1943+140_1943+141del
XM_011543481.2:c.1943+140_1943+141del	XP_011541783.1:n.1943+140_1943+141del
XM_011543484.2:c.1943+140_1943+141del	XP_011541786.1:n.1943+140_1943+141del
XM_011543485.2:c.1943+140_1943+141del	XP_011541787.1:n.1943+140_1943+141del
XM_011543486.3:c.1943+140_1943+141del	XP_011541788.1:n.1943+140_1943+141del
XM_017009581.1:c.1943+140_1943+141del	XP_016865070.1:n.1943+140_1943+141del
XM_017009583.2:c.848+140_848+141del	XP_016865072.1:n.848+140_848+141del
XM_024446113.1:c.1943+140_1943+141del	XP_024301881.1:n.1943+140_1943+141del
XR_001742119.2:n.2081+140_2081+141del
XR_001742445.1:n.3604_3605del
XR_001742446.1:n.1367_1368del
NM_001040458.3:c.1943+140_1943+141del MANE Select	NP_001035548.1:n.1943+140_1943+141del
NM_001198541.3:c.1943+140_1943+141del	NP_001185470.1:n.1943+140_1943+141del
NM_001349244.2:c.1943+140_1943+141del	NP_001336173.1:n.1943+140_1943+141del
NM_016442.5:c.1943+140_1943+141del	NP_057526.3:n.1943+140_1943+141del