Canonical Allele Identifier: CA360495385

Gene: ERAP1

Linked Data

• MyVariant Identifiers: chr5:g.96139124G>A (hg19) ; chr5:g.96803421G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96803421G>A , CM000667.2:g.96803421G>A	GRCh38
NC_000005.9:g.96139124G>A , CM000667.1:g.96139124G>A	GRCh37
NC_000005.8:g.96164880G>A	NCBI36
NG_027839.1:g.15725C>T
NG_027839.2:g.137563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443439.7:c.506C>T MANE Select	ENSP00000406304.2:p.Thr169Ile
ENST00000296754.7:c.506C>T	ENSP00000296754.3:p.Thr169Ile
ENST00000443439.6:c.506C>T	ENSP00000406304.2:p.Thr169Ile
ENST00000503921.5:c.-79C>T	ENSP00000427025.1:n.-79C>T
ENST00000508227.5:c.-59C>T	ENSP00000422631.1:n.-59C>T
NM_001040458.1:c.506C>T	NP_001035548.1:p.Thr169Ile
NM_001198541.1:c.506C>T	NP_001185470.1:p.Thr169Ile
NM_016442.3:c.506C>T	NP_057526.3:p.Thr169Ile
XM_005272015.3:c.506C>T	XP_005272072.1:p.Thr169Ile
XM_005272016.3:c.506C>T	XP_005272073.1:p.Thr169Ile
XM_011543480.1:c.506C>T	XP_011541782.1:p.Thr169Ile
XM_011543481.1:c.506C>T	XP_011541783.1:p.Thr169Ile
XM_011543482.1:c.506C>T	XP_011541784.1:p.Thr169Ile
XM_011543483.1:c.506C>T	XP_011541785.1:p.Thr169Ile
XM_011543484.1:c.506C>T	XP_011541786.1:p.Thr169Ile
XM_011543485.1:c.506C>T	XP_011541787.1:p.Thr169Ile
XM_011543486.1:c.506C>T	XP_011541788.1:p.Thr169Ile
XM_011543487.1:c.506C>T	XP_011541789.1:p.Thr169Ile
NM_001040458.2:c.506C>T	NP_001035548.1:p.Thr169Ile
NM_001198541.2:c.506C>T	NP_001185470.1:p.Thr169Ile
NM_001349244.1:c.506C>T	NP_001336173.1:p.Thr169Ile
NM_016442.4:c.506C>T	NP_057526.3:p.Thr169Ile
XM_005272015.5:c.506C>T	XP_005272072.1:p.Thr169Ile
XM_005272016.4:c.506C>T	XP_005272073.1:p.Thr169Ile
XM_011543480.2:c.506C>T	XP_011541782.1:p.Thr169Ile
XM_011543481.2:c.506C>T	XP_011541783.1:p.Thr169Ile
XM_011543484.2:c.506C>T	XP_011541786.1:p.Thr169Ile
XM_011543485.2:c.506C>T	XP_011541787.1:p.Thr169Ile
XM_011543486.3:c.506C>T	XP_011541788.1:p.Thr169Ile
XM_017009581.1:c.506C>T	XP_016865070.1:p.Thr169Ile
XM_017009583.2:c.-537C>T	XP_016865072.1:n.-537C>T
XM_024446113.1:c.506C>T	XP_024301881.1:p.Thr169Ile
XR_001742119.2:n.799C>T
NM_001040458.3:c.506C>T MANE Select	NP_001035548.1:p.Thr169Ile
NM_001198541.3:c.506C>T	NP_001185470.1:p.Thr169Ile
NM_001349244.2:c.506C>T	NP_001336173.1:p.Thr169Ile
NM_016442.5:c.506C>T	NP_057526.3:p.Thr169Ile