Canonical Allele Identifier: CA1139665231
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 917229
ClinVar RCV Id: RCV001173922
dbSNP Id: rs1907117054

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15239547_15239552del , CM000679.2:g.15239547_15239552del GRCh38
NC_000017.10:g.15142864_15142869del , CM000679.1:g.15142864_15142869del GRCh37
NC_000017.9:g.15083589_15083594del NCBI36
NG_007949.1:g.30782_30787del , LRG_263:g.30782_30787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.244_249del MANE Select ENSP00000308937.3:p.Leu82_Phe83del
ENST00000395936.7:c.244_249del ENSP00000379268.1:p.Leu82_Phe83del
ENST00000395938.7:c.233_238del ENSP00000379269.3:p.Pro78_Val79del
ENST00000426385.4:c.244_249del ENSP00000409824.3:p.Leu82_Phe83del
ENST00000494511.7:c.40_45del ENSP00000462782.2:p.Leu14_Phe15del
ENST00000580584.3:c.40_45del ENSP00000464468.3:p.Leu14_Phe15del
ENST00000612492.5:c.244_249del ENSP00000484631.1:p.Leu82_Phe83del
ENST00000643451.2:c.244_249del ENSP00000494628.1:p.Leu82_Phe83del
ENST00000644020.1:c.244_249del ENSP00000496522.1:p.Leu82_Phe83del
ENST00000646419.2:c.244_249del ENSP00000494871.1:p.Leu82_Phe83del
ENST00000674651.1:c.244_249del ENSP00000501727.1:p.Leu82_Phe83del
ENST00000674673.1:c.244_249del ENSP00000501804.1:p.Leu82_Phe83del
ENST00000674707.1:c.40_45del ENSP00000502250.1:p.Leu14_Phe15del
ENST00000674868.1:c.244_249del ENSP00000502835.1:p.Leu82_Phe83del
ENST00000674871.1:n.260_265del
ENST00000674947.1:c.233_238del ENSP00000501580.1:p.Pro78_Val79del
ENST00000675197.1:n.224_229del
ENST00000675350.1:c.244_249del ENSP00000501557.1:p.Leu82_Phe83del
ENST00000675551.1:c.244_249del ENSP00000501945.1:p.Leu82_Phe83del
ENST00000675808.1:c.244_249del ENSP00000502310.1:p.Leu82_Phe83del
ENST00000675819.1:c.244_249del ENSP00000502018.1:p.Leu82_Phe83del
ENST00000675854.1:c.40_45del ENSP00000502324.1:p.Leu14_Phe15del
ENST00000675950.1:c.244_249del ENSP00000501546.1:p.Leu82_Phe83del
ENST00000676161.1:c.179-8466_179-8461del ENSP00000501766.1:n.179-8466_179-8461del
ENST00000676221.1:c.244_249del ENSP00000502601.1:p.Leu82_Phe83del
ENST00000676329.1:c.346_351del ENSP00000501698.1:p.Leu116_Phe117del
ENST00000312280.7:c.244_249del ENSP00000308937.3:p.Leu82_Phe83del
ENST00000395936.5:c.244_249del ENSP00000379268.1:p.Leu82_Phe83del
ENST00000395938.6:c.244_249del ENSP00000379269.2:p.Leu82_Phe83del
ENST00000426385.3:c.244_249del ENSP00000409824.3:p.Leu82_Phe83del
ENST00000494511.5:c.65_70del ENSP00000462782.1:p.Pro22_Val23del
ENST00000580584.1:c.65_70del ENSP00000464468.1:p.Pro22_Val23del
ENST00000612492.4:c.244_249del ENSP00000484631.1:p.Leu82_Phe83del
NM_000304.3:c.244_249del NP_000295.1:p.Leu82_Phe83del
NM_001281455.1:c.244_249del NP_001268384.1:p.Leu82_Phe83del
NM_001281456.1:c.244_249del NP_001268385.1:p.Leu82_Phe83del
NM_153321.2:c.244_249del NP_696996.1:p.Leu82_Phe83del
NM_153322.2:c.244_249del NP_696997.1:p.Leu82_Phe83del
NR_104017.1:n.370_375del
NR_104018.1:n.270_275del
XM_011523943.1:c.244_249del XP_011522245.1:p.Leu82_Phe83del
NM_001330143.1:c.244_249del NP_001317072.1:p.Leu82_Phe83del
XM_024450806.1:c.244_249del XP_024306574.1:p.Leu82_Phe83del
NM_000304.4:c.244_249del MANE Select NP_000295.1:p.Leu82_Phe83del
NM_001281456.2:c.244_249del NP_001268385.1:p.Leu82_Phe83del
NM_001330143.2:c.244_249del NP_001317072.1:p.Leu82_Phe83del
NM_153321.3:c.244_249del NP_696996.1:p.Leu82_Phe83del
NM_153322.3:c.244_249del NP_696997.1:p.Leu82_Phe83del
NR_104017.2:n.339_344del
NR_104018.2:n.239_244del
NM_001281455.2:c.244_249del NP_001268384.1:p.Leu82_Phe83del