Canonical Allele Identifier: CA1565638058

Linked Data

dbSNP Id: rs1363907

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96917099G>C , CM000667.2:g.96917099G>C GRCh38
NC_000005.9:g.96252803G>C , CM000667.1:g.96252803G>C GRCh37
NC_000005.8:g.96278559G>C NCBI36
NG_027839.2:g.23885C>G
NG_051092.1:g.46161G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000510373.6:c.2740-363G>C (ERAP2) ENSP00000421175.2:n.2740-363G>C
ENST00000437043.8:c.2740-363G>C (ERAP2) MANE Select ENSP00000400376.3:n.2740-363G>C
ENST00000379904.8:c.2605-363G>C (ERAP2) ENSP00000369235.4:n.2605-363G>C
ENST00000437043.7:c.2740-363G>C (ERAP2) ENSP00000400376.3:n.2740-363G>C
ENST00000513084.5:c.*1242-363G>C (ERAP2) ENSP00000421849.1:n.*1242-363G>C
NM_001130140.1:c.2740-363G>C (ERAP2) NP_001123612.1:n.2740-363G>C
NM_022350.3:c.2740-363G>C (ERAP2) NP_071745.1:n.2740-363G>C
XM_011543480.1:c.-706+17023C>G (ERAP1) XP_011541782.1:n.-706+17023C>G
XM_011543481.1:c.-703+17023C>G (ERAP1) XP_011541783.1:n.-703+17023C>G
XM_011543482.1:c.-710+17023C>G (ERAP1) XP_011541784.1:n.-710+17023C>G
XM_011543483.1:c.-873+17023C>G (ERAP1) XP_011541785.1:n.-873+17023C>G
XM_011543484.1:c.-702+17023C>G (ERAP1) XP_011541786.1:n.-702+17023C>G
XM_011543485.1:c.-522+17023C>G (ERAP1) XP_011541787.1:n.-522+17023C>G
XM_011543486.1:c.-706+17023C>G (ERAP1) XP_011541788.1:n.-706+17023C>G
XM_011543487.1:c.-706+17023C>G (ERAP1) XP_011541789.1:n.-706+17023C>G
XM_011543544.1:c.2671-363G>C (ERAP2) XP_011541846.1:n.2671-363G>C
NM_001130140.2:c.2740-363G>C (ERAP2) NP_001123612.1:n.2740-363G>C
NM_001329229.1:c.2605-363G>C (ERAP2) NP_001316158.1:n.2605-363G>C
NM_022350.4:c.2740-363G>C (ERAP2) NP_071745.1:n.2740-363G>C
NR_137637.1:n.3552-363G>C (ERAP2)
XM_011543480.2:c.-706+17023C>G (ERAP1) XP_011541782.1:n.-706+17023C>G
XM_011543481.2:c.-703+17023C>G (ERAP1) XP_011541783.1:n.-703+17023C>G
XM_011543484.2:c.-702+17023C>G (ERAP1) XP_011541786.1:n.-702+17023C>G
XM_011543485.2:c.-522+17023C>G (ERAP1) XP_011541787.1:n.-522+17023C>G
XM_011543486.3:c.-706+17023C>G (ERAP1) XP_011541788.1:n.-706+17023C>G
XM_011543544.2:c.2671-363G>C (ERAP2) XP_011541846.1:n.2671-363G>C
XM_017009581.1:c.-548+17023C>G (ERAP1) XP_016865070.1:n.-548+17023C>G
XM_024446113.1:c.-545+17023C>G (ERAP1) XP_024301881.1:n.-545+17023C>G
XR_001742179.2:n.2953-363G>C (ERAP2)
NM_022350.5:c.2740-363G>C (ERAP2) MANE Select NP_071745.1:n.2740-363G>C