Canonical Allele Identifier: CA2249497522
Gene: PMP22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15230801_15230802delinsTG , CM000679.2:g.15230801_15230802delinsTG GRCh38
NC_000017.10:g.15134118_15134119delinsTG , CM000679.1:g.15134118_15134119delinsTG GRCh37
NC_000017.9:g.15074843_15074844delinsTG NCBI36
NG_007949.1:g.39526_39527delinsCA , LRG_263:g.39526_39527delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.*115_*116delinsCA MANE Select ENSP00000308937.3:n.*115_*116delinsCA
ENST00000395936.7:c.*307_*308delinsCA ENSP00000379268.1:n.*307_*308delinsCA
ENST00000395938.7:c.587_588delinsCA ENSP00000379269.3:p.Pro196=
ENST00000494511.7:c.*115_*116delinsCA ENSP00000462782.2:n.*115_*116delinsCA
ENST00000580584.3:c.*115_*116delinsCA ENSP00000464468.3:n.*115_*116delinsCA
ENST00000612492.5:c.*115_*116delinsCA ENSP00000484631.1:n.*115_*116delinsCA
ENST00000643451.2:c.*453_*454delinsCA ENSP00000494628.1:n.*453_*454delinsCA
ENST00000644020.1:c.*307_*308delinsCA ENSP00000496522.1:n.*307_*308delinsCA
ENST00000646419.2:c.*307_*308delinsCA ENSP00000494871.1:n.*307_*308delinsCA
ENST00000674651.1:c.*115_*116delinsCA ENSP00000501727.1:n.*115_*116delinsCA
ENST00000674673.1:c.*115_*116delinsCA ENSP00000501804.1:n.*115_*116delinsCA
ENST00000674707.1:c.*115_*116delinsCA ENSP00000502250.1:n.*115_*116delinsCA
ENST00000674868.1:c.*115_*116delinsCA ENSP00000502835.1:n.*115_*116delinsCA
ENST00000674871.1:n.614_615delinsCA
ENST00000674947.1:c.587_588delinsCA ENSP00000501580.1:p.Pro196=
ENST00000675197.1:n.578_579delinsCA
ENST00000675350.1:c.*115_*116delinsCA ENSP00000501557.1:n.*115_*116delinsCA
ENST00000675551.1:c.*267_*268delinsCA ENSP00000501945.1:n.*267_*268delinsCA
ENST00000675808.1:c.*115_*116delinsCA ENSP00000502310.1:n.*115_*116delinsCA
ENST00000675819.1:c.*115_*116delinsCA ENSP00000502018.1:n.*115_*116delinsCA
ENST00000675854.1:c.*115_*116delinsCA ENSP00000502324.1:n.*115_*116delinsCA
ENST00000675950.1:c.*115_*116delinsCA ENSP00000501546.1:n.*115_*116delinsCA
ENST00000676002.1:n.591_592delinsCA
ENST00000676161.1:c.*115_*116delinsCA ENSP00000501766.1:n.*115_*116delinsCA
ENST00000676221.1:c.*115_*116delinsCA ENSP00000502601.1:n.*115_*116delinsCA
ENST00000676329.1:c.*115_*116delinsCA ENSP00000501698.1:n.*115_*116delinsCA
ENST00000312280.7:c.*115_*116delinsCA ENSP00000308937.3:n.*115_*116delinsCA
ENST00000395936.5:c.*307_*308delinsCA ENSP00000379268.1:n.*307_*308delinsCA
ENST00000395938.6:c.*115_*116delinsCA ENSP00000379269.2:n.*115_*116delinsCA
ENST00000494511.5:c.419_420delinsCA ENSP00000462782.1:p.Pro140=
ENST00000612492.4:c.*115_*116delinsCA ENSP00000484631.1:n.*115_*116delinsCA
NM_000304.3:c.*115_*116delinsCA NP_000295.1:n.*115_*116delinsCA
NM_001281455.1:c.*115_*116delinsCA NP_001268384.1:n.*115_*116delinsCA
NM_001281456.1:c.*115_*116delinsCA NP_001268385.1:n.*115_*116delinsCA
NM_153321.2:c.*115_*116delinsCA NP_696996.1:n.*115_*116delinsCA
NM_153322.2:c.*115_*116delinsCA NP_696997.1:n.*115_*116delinsCA
NR_104017.1:n.724_725delinsCA
NR_104018.1:n.624_625delinsCA
NM_000304.4:c.*115_*116delinsCA MANE Select NP_000295.1:n.*115_*116delinsCA
NM_001281456.2:c.*115_*116delinsCA NP_001268385.1:n.*115_*116delinsCA
NM_153321.3:c.*115_*116delinsCA NP_696996.1:n.*115_*116delinsCA
NM_153322.3:c.*115_*116delinsCA NP_696997.1:n.*115_*116delinsCA
NR_104017.2:n.693_694delinsCA
NR_104018.2:n.593_594delinsCA
NM_001281455.2:c.*115_*116delinsCA NP_001268384.1:n.*115_*116delinsCA