Canonical Allele Identifier: CA398739582

Gene: PMP22

Linked Data

• ClinVar Variation Id: 448091
• ClinVar RCV Id: RCV000518626 ; RCV000658337 ; RCV001851451
• dbSNP Id: rs1555564040
• MyVariant Identifiers: chr17:g.15134299A>G (hg19) ; chr17:g.15230982A>G (hg38)
• PubMed: PMID:11545686

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230982A>G , CM000679.2:g.15230982A>G	GRCh38
NC_000017.10:g.15134299A>G , CM000679.1:g.15134299A>G	GRCh37
NC_000017.9:g.15075024A>G	NCBI36
NG_007949.1:g.39346T>C , LRG_263:g.39346T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.418T>C MANE Select	ENSP00000308937.3:p.Trp140Arg
ENST00000395936.7:c.*127T>C	ENSP00000379268.1:n.*127T>C
ENST00000395938.7:c.407T>C	ENSP00000379269.3:p.Leu136Pro
ENST00000494511.7:c.214T>C	ENSP00000462782.2:p.Trp72Arg
ENST00000580584.3:c.214T>C	ENSP00000464468.3:p.Trp72Arg
ENST00000612492.5:c.418T>C	ENSP00000484631.1:p.Trp140Arg
ENST00000643451.2:c.*273T>C	ENSP00000494628.1:n.*273T>C
ENST00000644020.1:c.*127T>C	ENSP00000496522.1:n.*127T>C
ENST00000646419.2:c.*127T>C	ENSP00000494871.1:n.*127T>C
ENST00000674651.1:c.418T>C	ENSP00000501727.1:p.Trp140Arg
ENST00000674673.1:c.418T>C	ENSP00000501804.1:p.Trp140Arg
ENST00000674707.1:c.214T>C	ENSP00000502250.1:p.Trp72Arg
ENST00000674868.1:c.418T>C	ENSP00000502835.1:p.Trp140Arg
ENST00000674871.1:n.434T>C
ENST00000674947.1:c.407T>C	ENSP00000501580.1:p.Leu136Pro
ENST00000675197.1:n.398T>C
ENST00000675350.1:c.418T>C	ENSP00000501557.1:p.Trp140Arg
ENST00000675551.1:c.*87T>C	ENSP00000501945.1:n.*87T>C
ENST00000675808.1:c.418T>C	ENSP00000502310.1:p.Trp140Arg
ENST00000675819.1:c.418T>C	ENSP00000502018.1:p.Trp140Arg
ENST00000675854.1:c.214T>C	ENSP00000502324.1:p.Trp72Arg
ENST00000675950.1:c.418T>C	ENSP00000501546.1:p.Trp140Arg
ENST00000676002.1:n.411T>C
ENST00000676161.1:c.277T>C	ENSP00000501766.1:p.Trp93Arg
ENST00000676221.1:c.418T>C	ENSP00000502601.1:p.Trp140Arg
ENST00000676329.1:c.520T>C	ENSP00000501698.1:p.Trp174Arg
ENST00000312280.7:c.418T>C	ENSP00000308937.3:p.Trp140Arg
ENST00000395936.5:c.*127T>C	ENSP00000379268.1:n.*127T>C
ENST00000395938.6:c.418T>C	ENSP00000379269.2:p.Trp140Arg
ENST00000494511.5:c.239T>C	ENSP00000462782.1:p.Leu80Pro
ENST00000612492.4:c.418T>C	ENSP00000484631.1:p.Trp140Arg
NM_000304.3:c.418T>C	NP_000295.1:p.Trp140Arg
NM_001281455.1:c.418T>C	NP_001268384.1:p.Trp140Arg
NM_001281456.1:c.418T>C	NP_001268385.1:p.Trp140Arg
NM_153321.2:c.418T>C	NP_696996.1:p.Trp140Arg
NM_153322.2:c.418T>C	NP_696997.1:p.Trp140Arg
NR_104017.1:n.544T>C
NR_104018.1:n.444T>C
NM_000304.4:c.418T>C MANE Select	NP_000295.1:p.Trp140Arg
NM_001281456.2:c.418T>C	NP_001268385.1:p.Trp140Arg
NM_153321.3:c.418T>C	NP_696996.1:p.Trp140Arg
NM_153322.3:c.418T>C	NP_696997.1:p.Trp140Arg
NR_104017.2:n.513T>C
NR_104018.2:n.413T>C
NM_001281455.2:c.418T>C	NP_001268384.1:p.Trp140Arg