Canonical Allele Identifier: CA1079049197

Gene: ERAP1

Linked Data

• dbSNP Id: rs1775895253
• gnomAD v3: 5-96785666-T-TG
• gnomAD v4: 5-96785666-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96785666_96785667insG , CM000667.2:g.96785666_96785667insG	GRCh38
NC_000005.9:g.96121370_96121371insG , CM000667.1:g.96121370_96121371insG	GRCh37
NC_000005.8:g.96147126_96147127insG	NCBI36
NG_027839.1:g.33478_33479insC
NG_027839.2:g.155317_155318insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.1943+121_1943+122insC MANE Select	ENSP00000406304.2:n.1943+121_1943+122insC
ENST00000296754.7:c.1943+121_1943+122insC	ENSP00000296754.3:n.1943+121_1943+122insC
ENST00000443439.6:c.1943+121_1943+122insC	ENSP00000406304.2:n.1943+121_1943+122insC
ENST00000507859.1:n.727_728insC
ENST00000514604.5:n.367+121_367+122insC
NM_001040458.1:c.1943+121_1943+122insC	NP_001035548.1:n.1943+121_1943+122insC
NM_001198541.1:c.1943+121_1943+122insC	NP_001185470.1:n.1943+121_1943+122insC
NM_016442.3:c.1943+121_1943+122insC	NP_057526.3:n.1943+121_1943+122insC
XM_005272015.3:c.1943+121_1943+122insC	XP_005272072.1:n.1943+121_1943+122insC
XM_005272016.3:c.1943+121_1943+122insC	XP_005272073.1:n.1943+121_1943+122insC
XM_011543480.1:c.1943+121_1943+122insC	XP_011541782.1:n.1943+121_1943+122insC
XM_011543481.1:c.1943+121_1943+122insC	XP_011541783.1:n.1943+121_1943+122insC
XM_011543482.1:c.1943+121_1943+122insC	XP_011541784.1:n.1943+121_1943+122insC
XM_011543483.1:c.1943+121_1943+122insC	XP_011541785.1:n.1943+121_1943+122insC
XM_011543484.1:c.1943+121_1943+122insC	XP_011541786.1:n.1943+121_1943+122insC
XM_011543485.1:c.1943+121_1943+122insC	XP_011541787.1:n.1943+121_1943+122insC
XM_011543486.1:c.1943+121_1943+122insC	XP_011541788.1:n.1943+121_1943+122insC
XM_011543487.1:c.1943+121_1943+122insC	XP_011541789.1:n.1943+121_1943+122insC
XR_427744.2:n.434_435insG
XR_948592.1:n.750_751insG
XR_948593.1:n.1058_1059insG
XR_948594.1:n.732_733insG
XR_948595.1:n.742_743insG
NM_001040458.2:c.1943+121_1943+122insC	NP_001035548.1:n.1943+121_1943+122insC
NM_001198541.2:c.1943+121_1943+122insC	NP_001185470.1:n.1943+121_1943+122insC
NM_001349244.1:c.1943+121_1943+122insC	NP_001336173.1:n.1943+121_1943+122insC
NM_016442.4:c.1943+121_1943+122insC	NP_057526.3:n.1943+121_1943+122insC
XM_005272015.5:c.1943+121_1943+122insC	XP_005272072.1:n.1943+121_1943+122insC
XM_005272016.4:c.1943+121_1943+122insC	XP_005272073.1:n.1943+121_1943+122insC
XM_011543480.2:c.1943+121_1943+122insC	XP_011541782.1:n.1943+121_1943+122insC
XM_011543481.2:c.1943+121_1943+122insC	XP_011541783.1:n.1943+121_1943+122insC
XM_011543484.2:c.1943+121_1943+122insC	XP_011541786.1:n.1943+121_1943+122insC
XM_011543485.2:c.1943+121_1943+122insC	XP_011541787.1:n.1943+121_1943+122insC
XM_011543486.3:c.1943+121_1943+122insC	XP_011541788.1:n.1943+121_1943+122insC
XM_017009581.1:c.1943+121_1943+122insC	XP_016865070.1:n.1943+121_1943+122insC
XM_017009583.2:c.848+121_848+122insC	XP_016865072.1:n.848+121_848+122insC
XM_024446113.1:c.1943+121_1943+122insC	XP_024301881.1:n.1943+121_1943+122insC
XR_001742119.2:n.2081+121_2081+122insC
XR_001742445.1:n.3623_3624insG
XR_001742446.1:n.1386_1387insG
NM_001040458.3:c.1943+121_1943+122insC MANE Select	NP_001035548.1:n.1943+121_1943+122insC
NM_001198541.3:c.1943+121_1943+122insC	NP_001185470.1:n.1943+121_1943+122insC
NM_001349244.2:c.1943+121_1943+122insC	NP_001336173.1:n.1943+121_1943+122insC
NM_016442.5:c.1943+121_1943+122insC	NP_057526.3:n.1943+121_1943+122insC