Canonical Allele Identifier: CA398739404

Gene: PMP22

Linked Data

• MyVariant Identifiers: chr17:g.15134231G>T (hg19) ; chr17:g.15230914G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230914G>T , CM000679.2:g.15230914G>T	GRCh38
NC_000017.10:g.15134231G>T , CM000679.1:g.15134231G>T	GRCh37
NC_000017.9:g.15074956G>T	NCBI36
NG_007949.1:g.39414C>A , LRG_263:g.39414C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.*3C>A MANE Select	ENSP00000308937.3:n.*3C>A
ENST00000395936.7:c.*195C>A	ENSP00000379268.1:n.*195C>A
ENST00000395938.7:c.475C>A	ENSP00000379269.3:p.Arg159Ser
ENST00000494511.7:c.*3C>A	ENSP00000462782.2:n.*3C>A
ENST00000580584.3:c.*3C>A	ENSP00000464468.3:n.*3C>A
ENST00000612492.5:c.*3C>A	ENSP00000484631.1:n.*3C>A
ENST00000643451.2:c.*341C>A	ENSP00000494628.1:n.*341C>A
ENST00000644020.1:c.*195C>A	ENSP00000496522.1:n.*195C>A
ENST00000646419.2:c.*195C>A	ENSP00000494871.1:n.*195C>A
ENST00000674651.1:c.*3C>A	ENSP00000501727.1:n.*3C>A
ENST00000674673.1:c.*3C>A	ENSP00000501804.1:n.*3C>A
ENST00000674707.1:c.*3C>A	ENSP00000502250.1:n.*3C>A
ENST00000674868.1:c.*3C>A	ENSP00000502835.1:n.*3C>A
ENST00000674871.1:n.502C>A
ENST00000674947.1:c.475C>A	ENSP00000501580.1:p.Arg159Ser
ENST00000675197.1:n.466C>A
ENST00000675350.1:c.*3C>A	ENSP00000501557.1:n.*3C>A
ENST00000675551.1:c.*155C>A	ENSP00000501945.1:n.*155C>A
ENST00000675808.1:c.*3C>A	ENSP00000502310.1:n.*3C>A
ENST00000675819.1:c.*3C>A	ENSP00000502018.1:n.*3C>A
ENST00000675854.1:c.*3C>A	ENSP00000502324.1:n.*3C>A
ENST00000675950.1:c.*3C>A	ENSP00000501546.1:n.*3C>A
ENST00000676002.1:n.479C>A
ENST00000676161.1:c.*3C>A	ENSP00000501766.1:n.*3C>A
ENST00000676221.1:c.*3C>A	ENSP00000502601.1:n.*3C>A
ENST00000676329.1:c.*3C>A	ENSP00000501698.1:n.*3C>A
ENST00000312280.7:c.*3C>A	ENSP00000308937.3:n.*3C>A
ENST00000395936.5:c.*195C>A	ENSP00000379268.1:n.*195C>A
ENST00000395938.6:c.*3C>A	ENSP00000379269.2:n.*3C>A
ENST00000494511.5:c.307C>A	ENSP00000462782.1:p.Arg103Ser
ENST00000612492.4:c.*3C>A	ENSP00000484631.1:n.*3C>A
NM_000304.3:c.*3C>A	NP_000295.1:n.*3C>A
NM_001281455.1:c.*3C>A	NP_001268384.1:n.*3C>A
NM_001281456.1:c.*3C>A	NP_001268385.1:n.*3C>A
NM_153321.2:c.*3C>A	NP_696996.1:n.*3C>A
NM_153322.2:c.*3C>A	NP_696997.1:n.*3C>A
NR_104017.1:n.612C>A
NR_104018.1:n.512C>A
NM_000304.4:c.*3C>A MANE Select	NP_000295.1:n.*3C>A
NM_001281456.2:c.*3C>A	NP_001268385.1:n.*3C>A
NM_153321.3:c.*3C>A	NP_696996.1:n.*3C>A
NM_153322.3:c.*3C>A	NP_696997.1:n.*3C>A
NR_104017.2:n.581C>A
NR_104018.2:n.481C>A
NM_001281455.2:c.*3C>A	NP_001268384.1:n.*3C>A