Canonical Allele Identifier: CA2695224548
Gene: PMP22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15239543dup , CM000679.2:g.15239543dup GRCh38
NC_000017.10:g.15142860dup , CM000679.1:g.15142860dup GRCh37
NC_000017.9:g.15083585dup NCBI36
NG_007949.1:g.30786dup , LRG_263:g.30786dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.248dup MANE Select ENSP00000308937.3:p.Phe84LeufsTer?
ENST00000395936.7:c.248dup ENSP00000379268.1:p.Phe84LeufsTer24
ENST00000395938.7:c.237dup ENSP00000379269.3:p.Leu80SerfsTer28
ENST00000426385.4:c.248dup ENSP00000409824.3:p.Phe84LeufsTer25
ENST00000494511.7:c.44dup ENSP00000462782.2:p.Phe16LeufsTer?
ENST00000580584.3:c.44dup ENSP00000464468.3:p.Phe16LeufsTer?
ENST00000612492.5:c.248dup ENSP00000484631.1:p.Phe84LeufsTer?
ENST00000643451.2:c.248dup ENSP00000494628.1:p.Phe84LeufsTer30
ENST00000644020.1:c.248dup ENSP00000496522.1:p.Phe84LeufsTer24
ENST00000646419.2:c.248dup ENSP00000494871.1:p.Phe84LeufsTer24
ENST00000674651.1:c.248dup ENSP00000501727.1:p.Phe84LeufsTer?
ENST00000674673.1:c.248dup ENSP00000501804.1:p.Phe84LeufsTer?
ENST00000674707.1:c.44dup ENSP00000502250.1:p.Phe16LeufsTer?
ENST00000674868.1:c.248dup ENSP00000502835.1:p.Phe84LeufsTer?
ENST00000674871.1:n.264dup
ENST00000674947.1:c.237dup ENSP00000501580.1:p.Leu80SerfsTer28
ENST00000675197.1:n.228dup
ENST00000675350.1:c.248dup ENSP00000501557.1:p.Phe84LeufsTer?
ENST00000675551.1:c.248dup ENSP00000501945.1:p.Phe84LeufsTer?
ENST00000675808.1:c.248dup ENSP00000502310.1:p.Phe84LeufsTer?
ENST00000675819.1:c.248dup ENSP00000502018.1:p.Phe84LeufsTer?
ENST00000675854.1:c.44dup ENSP00000502324.1:p.Phe16LeufsTer?
ENST00000675950.1:c.248dup ENSP00000501546.1:p.Phe84LeufsTer?
ENST00000676161.1:c.179-8462dup ENSP00000501766.1:n.179-8462dup
ENST00000676221.1:c.248dup ENSP00000502601.1:p.Phe84LeufsTer?
ENST00000676329.1:c.350dup ENSP00000501698.1:p.Phe118LeufsTer?
ENST00000312280.7:c.248dup ENSP00000308937.3:p.Phe84LeufsTer?
ENST00000395936.5:c.248dup ENSP00000379268.1:p.Phe84LeufsTer24
ENST00000395938.6:c.248dup ENSP00000379269.2:p.Phe84LeufsTer?
ENST00000426385.3:c.248dup ENSP00000409824.3:p.Phe84LeufsTer25
ENST00000494511.5:c.69dup ENSP00000462782.1:p.Leu24SerfsTer28
ENST00000580584.1:c.69dup ENSP00000464468.1:p.Leu24SerfsTer28
ENST00000612492.4:c.248dup ENSP00000484631.1:p.Phe84LeufsTer?
NM_000304.3:c.248dup NP_000295.1:p.Phe84LeufsTer?
NM_001281455.1:c.248dup NP_001268384.1:p.Phe84LeufsTer?
NM_001281456.1:c.248dup NP_001268385.1:p.Phe84LeufsTer?
NM_153321.2:c.248dup NP_696996.1:p.Phe84LeufsTer?
NM_153322.2:c.248dup NP_696997.1:p.Phe84LeufsTer?
NR_104017.1:n.374dup
NR_104018.1:n.274dup
XM_011523943.1:c.248dup XP_011522245.1:p.Phe84LeufsTer24
NM_001330143.1:c.248dup NP_001317072.1:p.Phe84LeufsTer24
XM_024450806.1:c.248dup XP_024306574.1:p.Phe84LeufsTer24
NM_000304.4:c.248dup MANE Select NP_000295.1:p.Phe84LeufsTer?
NM_001281456.2:c.248dup NP_001268385.1:p.Phe84LeufsTer?
NM_001330143.2:c.248dup NP_001317072.1:p.Phe84LeufsTer24
NM_153321.3:c.248dup NP_696996.1:p.Phe84LeufsTer?
NM_153322.3:c.248dup NP_696997.1:p.Phe84LeufsTer?
NR_104017.2:n.343dup
NR_104018.2:n.243dup
NM_001281455.2:c.248dup NP_001268384.1:p.Phe84LeufsTer?