Canonical Allele Identifier: CA2249497465

Gene: PMP22

Linked Data

• dbSNP Id: rs1906235707

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230778_15230779insAC , CM000679.2:g.15230778_15230779insAC	GRCh38
NC_000017.10:g.15134095_15134096insAC , CM000679.1:g.15134095_15134096insAC	GRCh37
NC_000017.9:g.15074820_15074821insAC	NCBI36
NG_007949.1:g.39550_39551insTG , LRG_263:g.39550_39551insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.*139_*140insTG MANE Select	ENSP00000308937.3:n.*139_*140insTG
ENST00000395936.7:c.*331_*332insTG	ENSP00000379268.1:n.*331_*332insTG
ENST00000395938.7:c.611_612insTG	ENSP00000379269.3:p.Leu205GlyfsTer4
ENST00000494511.7:c.*139_*140insTG	ENSP00000462782.2:n.*139_*140insTG
ENST00000580584.3:c.*139_*140insTG	ENSP00000464468.3:n.*139_*140insTG
ENST00000612492.5:c.*139_*140insTG	ENSP00000484631.1:n.*139_*140insTG
ENST00000643451.2:c.*477_*478insTG	ENSP00000494628.1:n.*477_*478insTG
ENST00000644020.1:c.*331_*332insTG	ENSP00000496522.1:n.*331_*332insTG
ENST00000646419.2:c.*331_*332insTG	ENSP00000494871.1:n.*331_*332insTG
ENST00000674651.1:c.*139_*140insTG	ENSP00000501727.1:n.*139_*140insTG
ENST00000674673.1:c.*139_*140insTG	ENSP00000501804.1:n.*139_*140insTG
ENST00000674707.1:c.*139_*140insTG	ENSP00000502250.1:n.*139_*140insTG
ENST00000674868.1:c.*139_*140insTG	ENSP00000502835.1:n.*139_*140insTG
ENST00000674871.1:n.638_639insTG
ENST00000674947.1:c.611_612insTG	ENSP00000501580.1:p.Leu205GlyfsTer4
ENST00000675197.1:n.602_603insTG
ENST00000675350.1:c.*139_*140insTG	ENSP00000501557.1:n.*139_*140insTG
ENST00000675551.1:c.*291_*292insTG	ENSP00000501945.1:n.*291_*292insTG
ENST00000675808.1:c.*139_*140insTG	ENSP00000502310.1:n.*139_*140insTG
ENST00000675819.1:c.*139_*140insTG	ENSP00000502018.1:n.*139_*140insTG
ENST00000675854.1:c.*139_*140insTG	ENSP00000502324.1:n.*139_*140insTG
ENST00000675950.1:c.*139_*140insTG	ENSP00000501546.1:n.*139_*140insTG
ENST00000676002.1:n.615_616insTG
ENST00000676161.1:c.*139_*140insTG	ENSP00000501766.1:n.*139_*140insTG
ENST00000676221.1:c.*139_*140insTG	ENSP00000502601.1:n.*139_*140insTG
ENST00000676329.1:c.*139_*140insTG	ENSP00000501698.1:n.*139_*140insTG
ENST00000312280.7:c.*139_*140insTG	ENSP00000308937.3:n.*139_*140insTG
ENST00000395938.6:c.*139_*140insTG	ENSP00000379269.2:n.*139_*140insTG
ENST00000494511.5:c.443_444insTG	ENSP00000462782.1:p.Leu149GlyfsTer4
ENST00000612492.4:c.*139_*140insTG	ENSP00000484631.1:n.*139_*140insTG
NM_000304.3:c.*139_*140insTG	NP_000295.1:n.*139_*140insTG
NM_001281455.1:c.*139_*140insTG	NP_001268384.1:n.*139_*140insTG
NM_001281456.1:c.*139_*140insTG	NP_001268385.1:n.*139_*140insTG
NM_153321.2:c.*139_*140insTG	NP_696996.1:n.*139_*140insTG
NM_153322.2:c.*139_*140insTG	NP_696997.1:n.*139_*140insTG
NR_104017.1:n.748_749insTG
NR_104018.1:n.648_649insTG
NM_000304.4:c.*139_*140insTG MANE Select	NP_000295.1:n.*139_*140insTG
NM_001281456.2:c.*139_*140insTG	NP_001268385.1:n.*139_*140insTG
NM_153321.3:c.*139_*140insTG	NP_696996.1:n.*139_*140insTG
NM_153322.3:c.*139_*140insTG	NP_696997.1:n.*139_*140insTG
NR_104017.2:n.717_718insTG
NR_104018.2:n.617_618insTG
NM_001281455.2:c.*139_*140insTG	NP_001268384.1:n.*139_*140insTG