Canonical Allele Identifier: CA2249498050
Gene: PMP22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15230979C= , CM000679.2:g.15230979C= GRCh38
NC_000017.10:g.15134296C= , CM000679.1:g.15134296C= GRCh37
NC_000017.9:g.15075021C= NCBI36
NG_007949.1:g.39349G= , LRG_263:g.39349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.421G= MANE Select ENSP00000308937.3:p.Val141=
ENST00000395936.7:c.*130G= ENSP00000379268.1:n.*130G=
ENST00000395938.7:c.410G= ENSP00000379269.3:p.Gly137=
ENST00000494511.7:c.217G= ENSP00000462782.2:p.Val73=
ENST00000580584.3:c.217G= ENSP00000464468.3:p.Val73=
ENST00000612492.5:c.421G= ENSP00000484631.1:p.Val141=
ENST00000643451.2:c.*276G= ENSP00000494628.1:n.*276G=
ENST00000644020.1:c.*130G= ENSP00000496522.1:n.*130G=
ENST00000646419.2:c.*130G= ENSP00000494871.1:n.*130G=
ENST00000674651.1:c.421G= ENSP00000501727.1:p.Val141=
ENST00000674673.1:c.421G= ENSP00000501804.1:p.Val141=
ENST00000674707.1:c.217G= ENSP00000502250.1:p.Val73=
ENST00000674868.1:c.421G= ENSP00000502835.1:p.Val141=
ENST00000674871.1:n.437G=
ENST00000674947.1:c.410G= ENSP00000501580.1:p.Gly137=
ENST00000675197.1:n.401G=
ENST00000675350.1:c.421G= ENSP00000501557.1:p.Val141=
ENST00000675551.1:c.*90G= ENSP00000501945.1:n.*90G=
ENST00000675808.1:c.421G= ENSP00000502310.1:p.Val141=
ENST00000675819.1:c.421G= ENSP00000502018.1:p.Val141=
ENST00000675854.1:c.217G= ENSP00000502324.1:p.Val73=
ENST00000675950.1:c.421G= ENSP00000501546.1:p.Val141=
ENST00000676002.1:n.414G=
ENST00000676161.1:c.280G= ENSP00000501766.1:p.Val94=
ENST00000676221.1:c.421G= ENSP00000502601.1:p.Val141=
ENST00000676329.1:c.523G= ENSP00000501698.1:p.Val175=
ENST00000312280.7:c.421G= ENSP00000308937.3:p.Val141=
ENST00000395936.5:c.*130G= ENSP00000379268.1:n.*130G=
ENST00000395938.6:c.421G= ENSP00000379269.2:p.Val141=
ENST00000494511.5:c.242G= ENSP00000462782.1:p.Gly81=
ENST00000612492.4:c.421G= ENSP00000484631.1:p.Val141=
NM_000304.3:c.421G= NP_000295.1:p.Val141=
NM_001281455.1:c.421G= NP_001268384.1:p.Val141=
NM_001281456.1:c.421G= NP_001268385.1:p.Val141=
NM_153321.2:c.421G= NP_696996.1:p.Val141=
NM_153322.2:c.421G= NP_696997.1:p.Val141=
NR_104017.1:n.547G=
NR_104018.1:n.447G=
NM_000304.4:c.421G= MANE Select NP_000295.1:p.Val141=
NM_001281456.2:c.421G= NP_001268385.1:p.Val141=
NM_153321.3:c.421G= NP_696996.1:p.Val141=
NM_153322.3:c.421G= NP_696997.1:p.Val141=
NR_104017.2:n.516G=
NR_104018.2:n.416G=
NM_001281455.2:c.421G= NP_001268384.1:p.Val141=