Canonical Allele Identifier: CA2628930316

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64156748dup , CM000677.2:g.64156748dup GRCh38
NC_000015.9:g.64448947dup , CM000677.1:g.64448947dup GRCh37
NC_000015.8:g.62236000dup NCBI36
NG_012979.1:g.11410dup , LRG_10:g.11410dup
NG_033071.1:g.10032dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.507dup (PPIB) MANE Select ENSP00000300026.4:p.Gly170TrpfsTer23
ENST00000325881.9:c.*2240dup (SNX22) MANE Select ENSP00000323435.4:n.*2240dup
ENST00000561048.2:n.3734dup (PPIB)
ENST00000680158.1:c.*180dup (PPIB) ENSP00000504873.1:n.*180dup
ENST00000680343.1:n.461dup (PPIB)
ENST00000681397.1:c.507dup (PPIB) ENSP00000506584.1:p.Gly170TrpfsTer23
ENST00000681658.1:c.402dup (PPIB) ENSP00000505431.1:p.Gly135TrpfsTer23
ENST00000300026.3:c.507dup (PPIB) ENSP00000300026.3:p.Gly170TrpfsTer23
ENST00000325881.8:c.*2240dup (SNX22) ENSP00000323435.4:n.*2240dup
ENST00000557789.5:n.2980dup (SNX22)
ENST00000560997.1:n.2635dup (SNX22)
NM_000942.4:c.507dup , LRG_10t1:c.507dup (PPIB) NP_000933.1:p.Gly170TrpfsTer23
NM_024798.2:c.*2240dup (SNX22) NP_079074.2:n.*2240dup
NR_073534.1:n.2928dup (SNX22)
XM_017022581.1:c.*2240dup (SNX22) XP_016878070.1:n.*2240dup
NM_024798.3:c.*2240dup (SNX22) MANE Select NP_079074.2:n.*2240dup
NM_000942.5:c.507dup (PPIB) MANE Select NP_000933.1:p.Gly170TrpfsTer23
NR_073534.2:n.2914dup (SNX22)