Canonical Allele Identifier: CA8403276

Gene: PMP22

Linked Data

• dbSNP Id: rs773958994
• ExAC: 17:15134155 TTTTCTTTGTCTGC / T
• gnomAD v2: 17-15134155-TTTTCTTTGTCTGC-T
• gnomAD v4: 17-15230838-TTTTCTTTGTCTGC-T
• MyVariant Identifiers: chr17:g.15134156_15134168del (hg19) ; chr17:g.15230839_15230851del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230844_15230856del , CM000679.2:g.15230844_15230856del	GRCh38
NC_000017.10:g.15134161_15134173del , CM000679.1:g.15134161_15134173del	GRCh37
NC_000017.9:g.15074886_15074898del	NCBI36
NG_007949.1:g.39477_39489del , LRG_263:g.39477_39489del

Transcript Alleles

HGVS	Amino-acid change
ENST00000312280.9:c.*66_*78del MANE Select	ENSP00000308937.3:n.*66_*78del
ENST00000395936.7:c.*258_*270del	ENSP00000379268.1:n.*258_*270del
ENST00000395938.7:c.538_550del	ENSP00000379269.3:p.Ala180LysfsTer24
ENST00000494511.7:c.*66_*78del	ENSP00000462782.2:n.*66_*78del
ENST00000580584.3:c.*66_*78del	ENSP00000464468.3:n.*66_*78del
ENST00000612492.5:c.*66_*78del	ENSP00000484631.1:n.*66_*78del
ENST00000643451.2:c.*404_*416del	ENSP00000494628.1:n.*404_*416del
ENST00000644020.1:c.*258_*270del	ENSP00000496522.1:n.*258_*270del
ENST00000646419.2:c.*258_*270del	ENSP00000494871.1:n.*258_*270del
ENST00000674651.1:c.*66_*78del	ENSP00000501727.1:n.*66_*78del
ENST00000674673.1:c.*66_*78del	ENSP00000501804.1:n.*66_*78del
ENST00000674707.1:c.*66_*78del	ENSP00000502250.1:n.*66_*78del
ENST00000674868.1:c.*66_*78del	ENSP00000502835.1:n.*66_*78del
ENST00000674871.1:n.565_577del
ENST00000674947.1:c.538_550del	ENSP00000501580.1:p.Ala180LysfsTer24
ENST00000675197.1:n.529_541del
ENST00000675350.1:c.*66_*78del	ENSP00000501557.1:n.*66_*78del
ENST00000675551.1:c.*218_*230del	ENSP00000501945.1:n.*218_*230del
ENST00000675808.1:c.*66_*78del	ENSP00000502310.1:n.*66_*78del
ENST00000675819.1:c.*66_*78del	ENSP00000502018.1:n.*66_*78del
ENST00000675854.1:c.*66_*78del	ENSP00000502324.1:n.*66_*78del
ENST00000675950.1:c.*66_*78del	ENSP00000501546.1:n.*66_*78del
ENST00000676002.1:n.542_554del
ENST00000676161.1:c.*66_*78del	ENSP00000501766.1:n.*66_*78del
ENST00000676221.1:c.*66_*78del	ENSP00000502601.1:n.*66_*78del
ENST00000676329.1:c.*66_*78del	ENSP00000501698.1:n.*66_*78del
ENST00000312280.7:c.*66_*78del	ENSP00000308937.3:n.*66_*78del
ENST00000395936.5:c.*258_*270del	ENSP00000379268.1:n.*258_*270del
ENST00000395938.6:c.*66_*78del	ENSP00000379269.2:n.*66_*78del
ENST00000494511.5:c.370_382del	ENSP00000462782.1:p.Ala124LysfsTer24
ENST00000612492.4:c.*66_*78del	ENSP00000484631.1:n.*66_*78del
NM_000304.3:c.*66_*78del	NP_000295.1:n.*66_*78del
NM_001281455.1:c.*66_*78del	NP_001268384.1:n.*66_*78del
NM_001281456.1:c.*66_*78del	NP_001268385.1:n.*66_*78del
NM_153321.2:c.*66_*78del	NP_696996.1:n.*66_*78del
NM_153322.2:c.*66_*78del	NP_696997.1:n.*66_*78del
NR_104017.1:n.675_687del
NR_104018.1:n.575_587del
NM_000304.4:c.*66_*78del MANE Select	NP_000295.1:n.*66_*78del
NM_001281456.2:c.*66_*78del	NP_001268385.1:n.*66_*78del
NM_153321.3:c.*66_*78del	NP_696996.1:n.*66_*78del
NM_153322.3:c.*66_*78del	NP_696997.1:n.*66_*78del
NR_104017.2:n.644_656del
NR_104018.2:n.544_556del
NM_001281455.2:c.*66_*78del	NP_001268384.1:n.*66_*78del