Canonical Allele Identifier: CA122964890

Gene: ERAP1

Linked Data

• dbSNP Id: rs869113108
• MyVariant Identifiers: chr5:g.96121374_96121375insA (hg19) ; chr5:g.96785670_96785671insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96785670_96785671insA , CM000667.2:g.96785670_96785671insA	GRCh38
NC_000005.9:g.96121374_96121375insA , CM000667.1:g.96121374_96121375insA	GRCh37
NC_000005.8:g.96147130_96147131insA	NCBI36
NG_027839.1:g.33474_33475insT
NG_027839.2:g.155313_155314insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.1943+117_1943+118insT MANE Select	ENSP00000406304.2:n.1943+117_1943+118insT
ENST00000296754.7:c.1943+117_1943+118insT	ENSP00000296754.3:n.1943+117_1943+118insT
ENST00000443439.6:c.1943+117_1943+118insT	ENSP00000406304.2:n.1943+117_1943+118insT
ENST00000507859.1:n.723_724insT
ENST00000514604.5:n.367+117_367+118insT
NM_001040458.1:c.1943+117_1943+118insT	NP_001035548.1:n.1943+117_1943+118insT
NM_001198541.1:c.1943+117_1943+118insT	NP_001185470.1:n.1943+117_1943+118insT
NM_016442.3:c.1943+117_1943+118insT	NP_057526.3:n.1943+117_1943+118insT
XM_005272015.3:c.1943+117_1943+118insT	XP_005272072.1:n.1943+117_1943+118insT
XM_005272016.3:c.1943+117_1943+118insT	XP_005272073.1:n.1943+117_1943+118insT
XM_011543480.1:c.1943+117_1943+118insT	XP_011541782.1:n.1943+117_1943+118insT
XM_011543481.1:c.1943+117_1943+118insT	XP_011541783.1:n.1943+117_1943+118insT
XM_011543482.1:c.1943+117_1943+118insT	XP_011541784.1:n.1943+117_1943+118insT
XM_011543483.1:c.1943+117_1943+118insT	XP_011541785.1:n.1943+117_1943+118insT
XM_011543484.1:c.1943+117_1943+118insT	XP_011541786.1:n.1943+117_1943+118insT
XM_011543485.1:c.1943+117_1943+118insT	XP_011541787.1:n.1943+117_1943+118insT
XM_011543486.1:c.1943+117_1943+118insT	XP_011541788.1:n.1943+117_1943+118insT
XM_011543487.1:c.1943+117_1943+118insT	XP_011541789.1:n.1943+117_1943+118insT
XR_427744.2:n.438_439insA
XR_948592.1:n.754_755insA
XR_948593.1:n.1062_1063insA
XR_948594.1:n.736_737insA
XR_948595.1:n.746_747insA
NM_001040458.2:c.1943+117_1943+118insT	NP_001035548.1:n.1943+117_1943+118insT
NM_001198541.2:c.1943+117_1943+118insT	NP_001185470.1:n.1943+117_1943+118insT
NM_001349244.1:c.1943+117_1943+118insT	NP_001336173.1:n.1943+117_1943+118insT
NM_016442.4:c.1943+117_1943+118insT	NP_057526.3:n.1943+117_1943+118insT
XM_005272015.5:c.1943+117_1943+118insT	XP_005272072.1:n.1943+117_1943+118insT
XM_005272016.4:c.1943+117_1943+118insT	XP_005272073.1:n.1943+117_1943+118insT
XM_011543480.2:c.1943+117_1943+118insT	XP_011541782.1:n.1943+117_1943+118insT
XM_011543481.2:c.1943+117_1943+118insT	XP_011541783.1:n.1943+117_1943+118insT
XM_011543484.2:c.1943+117_1943+118insT	XP_011541786.1:n.1943+117_1943+118insT
XM_011543485.2:c.1943+117_1943+118insT	XP_011541787.1:n.1943+117_1943+118insT
XM_011543486.3:c.1943+117_1943+118insT	XP_011541788.1:n.1943+117_1943+118insT
XM_017009581.1:c.1943+117_1943+118insT	XP_016865070.1:n.1943+117_1943+118insT
XM_017009583.2:c.848+117_848+118insT	XP_016865072.1:n.848+117_848+118insT
XM_024446113.1:c.1943+117_1943+118insT	XP_024301881.1:n.1943+117_1943+118insT
XR_001742119.2:n.2081+117_2081+118insT
XR_001742445.1:n.3627_3628insA
XR_001742446.1:n.1390_1391insA
NM_001040458.3:c.1943+117_1943+118insT MANE Select	NP_001035548.1:n.1943+117_1943+118insT
NM_001198541.3:c.1943+117_1943+118insT	NP_001185470.1:n.1943+117_1943+118insT
NM_001349244.2:c.1943+117_1943+118insT	NP_001336173.1:n.1943+117_1943+118insT
NM_016442.5:c.1943+117_1943+118insT	NP_057526.3:n.1943+117_1943+118insT