Canonical Allele Identifier: CA2249505932
Gene: PMP22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15239599G= , CM000679.2:g.15239599G= GRCh38
NC_000017.10:g.15142916G= , CM000679.1:g.15142916G= GRCh37
NC_000017.9:g.15083641G= NCBI36
NG_007949.1:g.30729C= , LRG_263:g.30729C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312280.9:c.191C= MANE Select ENSP00000308937.3:p.Ser64=
ENST00000395936.7:c.191C= ENSP00000379268.1:p.Ser64=
ENST00000395938.7:c.180C= ENSP00000379269.3:p.Val60=
ENST00000426385.4:c.191C= ENSP00000409824.3:p.Ser64=
ENST00000494511.7:c.-14C= ENSP00000462782.2:n.-14C=
ENST00000580584.3:c.-14C= ENSP00000464468.3:n.-14C=
ENST00000612492.5:c.191C= ENSP00000484631.1:p.Ser64=
ENST00000643451.2:c.191C= ENSP00000494628.1:p.Ser64=
ENST00000644020.1:c.191C= ENSP00000496522.1:p.Ser64=
ENST00000646419.2:c.191C= ENSP00000494871.1:p.Ser64=
ENST00000674651.1:c.191C= ENSP00000501727.1:p.Ser64=
ENST00000674673.1:c.191C= ENSP00000501804.1:p.Ser64=
ENST00000674707.1:c.-14C= ENSP00000502250.1:n.-14C=
ENST00000674868.1:c.191C= ENSP00000502835.1:p.Ser64=
ENST00000674871.1:n.207C=
ENST00000674947.1:c.180C= ENSP00000501580.1:p.Val60=
ENST00000675197.1:n.171C=
ENST00000675350.1:c.191C= ENSP00000501557.1:p.Ser64=
ENST00000675551.1:c.191C= ENSP00000501945.1:p.Ser64=
ENST00000675808.1:c.191C= ENSP00000502310.1:p.Ser64=
ENST00000675819.1:c.191C= ENSP00000502018.1:p.Ser64=
ENST00000675854.1:c.-14C= ENSP00000502324.1:n.-14C=
ENST00000675950.1:c.191C= ENSP00000501546.1:p.Ser64=
ENST00000676161.1:c.179-8519C= ENSP00000501766.1:n.179-8519C=
ENST00000676221.1:c.191C= ENSP00000502601.1:p.Ser64=
ENST00000676329.1:c.293C= ENSP00000501698.1:p.Ser98=
ENST00000312280.7:c.191C= ENSP00000308937.3:p.Ser64=
ENST00000395936.5:c.191C= ENSP00000379268.1:p.Ser64=
ENST00000395938.6:c.191C= ENSP00000379269.2:p.Ser64=
ENST00000426385.3:c.191C= ENSP00000409824.3:p.Ser64=
ENST00000494511.5:c.12C= ENSP00000462782.1:p.Val4=
ENST00000580584.1:c.12C= ENSP00000464468.1:p.Val4=
ENST00000612492.4:c.191C= ENSP00000484631.1:p.Ser64=
NM_000304.3:c.191C= NP_000295.1:p.Ser64=
NM_001281455.1:c.191C= NP_001268384.1:p.Ser64=
NM_001281456.1:c.191C= NP_001268385.1:p.Ser64=
NM_153321.2:c.191C= NP_696996.1:p.Ser64=
NM_153322.2:c.191C= NP_696997.1:p.Ser64=
NR_104017.1:n.317C=
NR_104018.1:n.217C=
XM_011523943.1:c.191C= XP_011522245.1:p.Ser64=
NM_001330143.1:c.191C= NP_001317072.1:p.Ser64=
XM_024450806.1:c.191C= XP_024306574.1:p.Ser64=
NM_000304.4:c.191C= MANE Select NP_000295.1:p.Ser64=
NM_001281456.2:c.191C= NP_001268385.1:p.Ser64=
NM_001330143.2:c.191C= NP_001317072.1:p.Ser64=
NM_153321.3:c.191C= NP_696996.1:p.Ser64=
NM_153322.3:c.191C= NP_696997.1:p.Ser64=
NR_104017.2:n.286C=
NR_104018.2:n.186C=
NM_001281455.2:c.191C= NP_001268384.1:p.Ser64=