Canonical Allele Identifier: CA11975653
Gene: ERAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96861018C>A , CM000667.2:g.96861018C>A GRCh38
NC_000005.9:g.96196721C>A , CM000667.1:g.96196721C>A GRCh37
NC_000005.8:g.96222477C>A NCBI36
NG_027839.2:g.79966G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011543480.1:c.-455+12268G>T XP_011541782.1:n.-455+12268G>T
XM_011543481.1:c.-452+12268G>T XP_011541783.1:n.-452+12268G>T
XM_011543482.1:c.-459+12268G>T XP_011541784.1:n.-459+12268G>T
XM_011543483.1:c.-622+12268G>T XP_011541785.1:n.-622+12268G>T
XM_011543484.1:c.-451+12268G>T XP_011541786.1:n.-451+12268G>T
XM_011543485.1:c.-271+12268G>T XP_011541787.1:n.-271+12268G>T
XM_011543486.1:c.-455+12268G>T XP_011541788.1:n.-455+12268G>T
XM_011543487.1:c.-455+12268G>T XP_011541789.1:n.-455+12268G>T
XM_011543480.2:c.-455+12268G>T XP_011541782.1:n.-455+12268G>T
XM_011543481.2:c.-452+12268G>T XP_011541783.1:n.-452+12268G>T
XM_011543484.2:c.-451+12268G>T XP_011541786.1:n.-451+12268G>T
XM_011543485.2:c.-271+12268G>T XP_011541787.1:n.-271+12268G>T
XM_011543486.3:c.-455+12268G>T XP_011541788.1:n.-455+12268G>T
XM_017009581.1:c.-455+12268G>T XP_016865070.1:n.-455+12268G>T
XM_024446113.1:c.-452+12268G>T XP_024301881.1:n.-452+12268G>T