Canonical Allele Identifier: CA915949573

Gene: PMP22

Linked Data

• ClinVar Variation Id: 637840
• ClinVar RCV Id: RCV000790170
• dbSNP Id: rs1597597443

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230958_15230959del , CM000679.2:g.15230958_15230959del	GRCh38
NC_000017.10:g.15134275_15134276del , CM000679.1:g.15134275_15134276del	GRCh37
NC_000017.9:g.15075000_15075001del	NCBI36
NG_007949.1:g.39371_39372del , LRG_263:g.39371_39372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.443_444del MANE Select	ENSP00000308937.3:p.Leu148GlnfsTer?
ENST00000395936.7:c.*152_*153del	ENSP00000379268.1:n.*152_*153del
ENST00000395938.7:c.432_433del	ENSP00000379269.3:p.Gln145AlafsTer6
ENST00000494511.7:c.239_240del	ENSP00000462782.2:p.Leu80GlnfsTer?
ENST00000580584.3:c.239_240del	ENSP00000464468.3:p.Leu80GlnfsTer?
ENST00000612492.5:c.443_444del	ENSP00000484631.1:p.Leu148GlnfsTer?
ENST00000643451.2:c.*298_*299del	ENSP00000494628.1:n.*298_*299del
ENST00000644020.1:c.*152_*153del	ENSP00000496522.1:n.*152_*153del
ENST00000646419.2:c.*152_*153del	ENSP00000494871.1:n.*152_*153del
ENST00000674651.1:c.443_444del	ENSP00000501727.1:p.Leu148GlnfsTer?
ENST00000674673.1:c.443_444del	ENSP00000501804.1:p.Leu148GlnfsTer?
ENST00000674707.1:c.239_240del	ENSP00000502250.1:p.Leu80GlnfsTer?
ENST00000674868.1:c.443_444del	ENSP00000502835.1:p.Leu148GlnfsTer?
ENST00000674871.1:n.459_460del
ENST00000674947.1:c.432_433del	ENSP00000501580.1:p.Gln145AlafsTer6
ENST00000675197.1:n.423_424del
ENST00000675350.1:c.443_444del	ENSP00000501557.1:p.Leu148GlnfsTer?
ENST00000675551.1:c.*112_*113del	ENSP00000501945.1:n.*112_*113del
ENST00000675808.1:c.443_444del	ENSP00000502310.1:p.Leu148GlnfsTer?
ENST00000675819.1:c.443_444del	ENSP00000502018.1:p.Leu148GlnfsTer?
ENST00000675854.1:c.239_240del	ENSP00000502324.1:p.Leu80GlnfsTer?
ENST00000675950.1:c.443_444del	ENSP00000501546.1:p.Leu148GlnfsTer?
ENST00000676002.1:n.436_437del
ENST00000676161.1:c.302_303del	ENSP00000501766.1:p.Leu101GlnfsTer?
ENST00000676221.1:c.443_444del	ENSP00000502601.1:p.Leu148GlnfsTer?
ENST00000676329.1:c.545_546del	ENSP00000501698.1:p.Leu182GlnfsTer?
ENST00000312280.7:c.443_444del	ENSP00000308937.3:p.Leu148GlnfsTer?
ENST00000395936.5:c.*152_*153del	ENSP00000379268.1:n.*152_*153del
ENST00000395938.6:c.443_444del	ENSP00000379269.2:p.Leu148GlnfsTer?
ENST00000494511.5:c.264_265del	ENSP00000462782.1:p.Gln89AlafsTer6
ENST00000612492.4:c.443_444del	ENSP00000484631.1:p.Leu148GlnfsTer?
NM_000304.3:c.443_444del	NP_000295.1:p.Leu148GlnfsTer?
NM_001281455.1:c.443_444del	NP_001268384.1:p.Leu148GlnfsTer?
NM_001281456.1:c.443_444del	NP_001268385.1:p.Leu148GlnfsTer?
NM_153321.2:c.443_444del	NP_696996.1:p.Leu148GlnfsTer?
NM_153322.2:c.443_444del	NP_696997.1:p.Leu148GlnfsTer?
NR_104017.1:n.569_570del
NR_104018.1:n.469_470del
NM_000304.4:c.443_444del MANE Select	NP_000295.1:p.Leu148GlnfsTer?
NM_001281456.2:c.443_444del	NP_001268385.1:p.Leu148GlnfsTer?
NM_153321.3:c.443_444del	NP_696996.1:p.Leu148GlnfsTer?
NM_153322.3:c.443_444del	NP_696997.1:p.Leu148GlnfsTer?
NR_104017.2:n.538_539del
NR_104018.2:n.438_439del
NM_001281455.2:c.443_444del	NP_001268384.1:p.Leu148GlnfsTer?