Canonical Allele Identifier: CA10577555

Gene: PMP22

Linked Data

• ClinVar Variation Id: 234605
• ClinVar RCV Id: RCV000213954 ; RCV000790160
• dbSNP Id: rs775019409
• MyVariant Identifiers: chr17:g.15134270G>T (hg19) ; chr17:g.15230953G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230953G>T , CM000679.2:g.15230953G>T	GRCh38
NC_000017.10:g.15134270G>T , CM000679.1:g.15134270G>T	GRCh37
NC_000017.9:g.15074995G>T	NCBI36
NG_007949.1:g.39375C>A , LRG_263:g.39375C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.447C>A MANE Select	ENSP00000308937.3:p.Ser149Arg
ENST00000395936.7:c.*156C>A	ENSP00000379268.1:n.*156C>A
ENST00000395938.7:c.436C>A	ENSP00000379269.3:p.Arg146=
ENST00000494511.7:c.243C>A	ENSP00000462782.2:p.Ser81Arg
ENST00000580584.3:c.243C>A	ENSP00000464468.3:p.Ser81Arg
ENST00000612492.5:c.447C>A	ENSP00000484631.1:p.Ser149Arg
ENST00000643451.2:c.*302C>A	ENSP00000494628.1:n.*302C>A
ENST00000644020.1:c.*156C>A	ENSP00000496522.1:n.*156C>A
ENST00000646419.2:c.*156C>A	ENSP00000494871.1:n.*156C>A
ENST00000674651.1:c.447C>A	ENSP00000501727.1:p.Ser149Arg
ENST00000674673.1:c.447C>A	ENSP00000501804.1:p.Ser149Arg
ENST00000674707.1:c.243C>A	ENSP00000502250.1:p.Ser81Arg
ENST00000674868.1:c.447C>A	ENSP00000502835.1:p.Ser149Arg
ENST00000674871.1:n.463C>A
ENST00000674947.1:c.436C>A	ENSP00000501580.1:p.Arg146=
ENST00000675197.1:n.427C>A
ENST00000675350.1:c.447C>A	ENSP00000501557.1:p.Ser149Arg
ENST00000675551.1:c.*116C>A	ENSP00000501945.1:n.*116C>A
ENST00000675808.1:c.447C>A	ENSP00000502310.1:p.Ser149Arg
ENST00000675819.1:c.447C>A	ENSP00000502018.1:p.Ser149Arg
ENST00000675854.1:c.243C>A	ENSP00000502324.1:p.Ser81Arg
ENST00000675950.1:c.447C>A	ENSP00000501546.1:p.Ser149Arg
ENST00000676002.1:n.440C>A
ENST00000676161.1:c.306C>A	ENSP00000501766.1:p.Ser102Arg
ENST00000676221.1:c.447C>A	ENSP00000502601.1:p.Ser149Arg
ENST00000676329.1:c.549C>A	ENSP00000501698.1:p.Ser183Arg
ENST00000312280.7:c.447C>A	ENSP00000308937.3:p.Ser149Arg
ENST00000395936.5:c.*156C>A	ENSP00000379268.1:n.*156C>A
ENST00000395938.6:c.447C>A	ENSP00000379269.2:p.Ser149Arg
ENST00000494511.5:c.268C>A	ENSP00000462782.1:p.Arg90=
ENST00000612492.4:c.447C>A	ENSP00000484631.1:p.Ser149Arg
NM_000304.3:c.447C>A	NP_000295.1:p.Ser149Arg
NM_001281455.1:c.447C>A	NP_001268384.1:p.Ser149Arg
NM_001281456.1:c.447C>A	NP_001268385.1:p.Ser149Arg
NM_153321.2:c.447C>A	NP_696996.1:p.Ser149Arg
NM_153322.2:c.447C>A	NP_696997.1:p.Ser149Arg
NR_104017.1:n.573C>A
NR_104018.1:n.473C>A
NM_000304.4:c.447C>A MANE Select	NP_000295.1:p.Ser149Arg
NM_001281456.2:c.447C>A	NP_001268385.1:p.Ser149Arg
NM_153321.3:c.447C>A	NP_696996.1:p.Ser149Arg
NM_153322.3:c.447C>A	NP_696997.1:p.Ser149Arg
NR_104017.2:n.542C>A
NR_104018.2:n.442C>A
NM_001281455.2:c.447C>A	NP_001268384.1:p.Ser149Arg