Canonical Allele Identifier: CA2249498141
Gene: PMP22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15230999A= , CM000679.2:g.15230999A= GRCh38
NC_000017.10:g.15134316A= , CM000679.1:g.15134316A= GRCh37
NC_000017.9:g.15075041A= NCBI36
NG_007949.1:g.39329T= , LRG_263:g.39329T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.401T= MANE Select ENSP00000308937.3:p.Phe134=
ENST00000395936.7:c.*110T= ENSP00000379268.1:n.*110T=
ENST00000395938.7:c.390T= ENSP00000379269.3:p.Phe130=
ENST00000494511.7:c.197T= ENSP00000462782.2:p.Phe66=
ENST00000580584.3:c.197T= ENSP00000464468.3:p.Phe66=
ENST00000612492.5:c.401T= ENSP00000484631.1:p.Phe134=
ENST00000643451.2:c.*256T= ENSP00000494628.1:n.*256T=
ENST00000644020.1:c.*110T= ENSP00000496522.1:n.*110T=
ENST00000646419.2:c.*110T= ENSP00000494871.1:n.*110T=
ENST00000674651.1:c.401T= ENSP00000501727.1:p.Phe134=
ENST00000674673.1:c.401T= ENSP00000501804.1:p.Phe134=
ENST00000674707.1:c.197T= ENSP00000502250.1:p.Phe66=
ENST00000674868.1:c.401T= ENSP00000502835.1:p.Phe134=
ENST00000674871.1:n.417T=
ENST00000674947.1:c.390T= ENSP00000501580.1:p.Phe130=
ENST00000675197.1:n.381T=
ENST00000675350.1:c.401T= ENSP00000501557.1:p.Phe134=
ENST00000675551.1:c.*70T= ENSP00000501945.1:n.*70T=
ENST00000675808.1:c.401T= ENSP00000502310.1:p.Phe134=
ENST00000675819.1:c.401T= ENSP00000502018.1:p.Phe134=
ENST00000675854.1:c.197T= ENSP00000502324.1:p.Phe66=
ENST00000675950.1:c.401T= ENSP00000501546.1:p.Phe134=
ENST00000676002.1:n.394T=
ENST00000676161.1:c.260T= ENSP00000501766.1:p.Phe87=
ENST00000676221.1:c.401T= ENSP00000502601.1:p.Phe134=
ENST00000676329.1:c.503T= ENSP00000501698.1:p.Phe168=
ENST00000312280.7:c.401T= ENSP00000308937.3:p.Phe134=
ENST00000395936.5:c.*110T= ENSP00000379268.1:n.*110T=
ENST00000395938.6:c.401T= ENSP00000379269.2:p.Phe134=
ENST00000494511.5:c.222T= ENSP00000462782.1:p.Phe74=
ENST00000612492.4:c.401T= ENSP00000484631.1:p.Phe134=
NM_000304.3:c.401T= NP_000295.1:p.Phe134=
NM_001281455.1:c.401T= NP_001268384.1:p.Phe134=
NM_001281456.1:c.401T= NP_001268385.1:p.Phe134=
NM_153321.2:c.401T= NP_696996.1:p.Phe134=
NM_153322.2:c.401T= NP_696997.1:p.Phe134=
NR_104017.1:n.527T=
NR_104018.1:n.427T=
NM_000304.4:c.401T= MANE Select NP_000295.1:p.Phe134=
NM_001281456.2:c.401T= NP_001268385.1:p.Phe134=
NM_153321.3:c.401T= NP_696996.1:p.Phe134=
NM_153322.3:c.401T= NP_696997.1:p.Phe134=
NR_104017.2:n.496T=
NR_104018.2:n.396T=
NM_001281455.2:c.401T= NP_001268384.1:p.Phe134=