Canonical Allele Identifier: CA398739330

Gene: PMP22

Linked Data

• MyVariant Identifiers: chr17:g.15134193C>A (hg19) ; chr17:g.15230876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15230876C>A , CM000679.2:g.15230876C>A	GRCh38
NC_000017.10:g.15134193C>A , CM000679.1:g.15134193C>A	GRCh37
NC_000017.9:g.15074918C>A	NCBI36
NG_007949.1:g.39452G>T , LRG_263:g.39452G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.*41G>T MANE Select	ENSP00000308937.3:n.*41G>T
ENST00000395936.7:c.*233G>T	ENSP00000379268.1:n.*233G>T
ENST00000395938.7:c.513G>T	ENSP00000379269.3:p.Arg171Ser
ENST00000494511.7:c.*41G>T	ENSP00000462782.2:n.*41G>T
ENST00000580584.3:c.*41G>T	ENSP00000464468.3:n.*41G>T
ENST00000612492.5:c.*41G>T	ENSP00000484631.1:n.*41G>T
ENST00000643451.2:c.*379G>T	ENSP00000494628.1:n.*379G>T
ENST00000644020.1:c.*233G>T	ENSP00000496522.1:n.*233G>T
ENST00000646419.2:c.*233G>T	ENSP00000494871.1:n.*233G>T
ENST00000674651.1:c.*41G>T	ENSP00000501727.1:n.*41G>T
ENST00000674673.1:c.*41G>T	ENSP00000501804.1:n.*41G>T
ENST00000674707.1:c.*41G>T	ENSP00000502250.1:n.*41G>T
ENST00000674868.1:c.*41G>T	ENSP00000502835.1:n.*41G>T
ENST00000674871.1:n.540G>T
ENST00000674947.1:c.513G>T	ENSP00000501580.1:p.Arg171Ser
ENST00000675197.1:n.504G>T
ENST00000675350.1:c.*41G>T	ENSP00000501557.1:n.*41G>T
ENST00000675551.1:c.*193G>T	ENSP00000501945.1:n.*193G>T
ENST00000675808.1:c.*41G>T	ENSP00000502310.1:n.*41G>T
ENST00000675819.1:c.*41G>T	ENSP00000502018.1:n.*41G>T
ENST00000675854.1:c.*41G>T	ENSP00000502324.1:n.*41G>T
ENST00000675950.1:c.*41G>T	ENSP00000501546.1:n.*41G>T
ENST00000676002.1:n.517G>T
ENST00000676161.1:c.*41G>T	ENSP00000501766.1:n.*41G>T
ENST00000676221.1:c.*41G>T	ENSP00000502601.1:n.*41G>T
ENST00000676329.1:c.*41G>T	ENSP00000501698.1:n.*41G>T
ENST00000312280.7:c.*41G>T	ENSP00000308937.3:n.*41G>T
ENST00000395936.5:c.*233G>T	ENSP00000379268.1:n.*233G>T
ENST00000395938.6:c.*41G>T	ENSP00000379269.2:n.*41G>T
ENST00000494511.5:c.345G>T	ENSP00000462782.1:p.Arg115Ser
ENST00000612492.4:c.*41G>T	ENSP00000484631.1:n.*41G>T
NM_000304.3:c.*41G>T	NP_000295.1:n.*41G>T
NM_001281455.1:c.*41G>T	NP_001268384.1:n.*41G>T
NM_001281456.1:c.*41G>T	NP_001268385.1:n.*41G>T
NM_153321.2:c.*41G>T	NP_696996.1:n.*41G>T
NM_153322.2:c.*41G>T	NP_696997.1:n.*41G>T
NR_104017.1:n.650G>T
NR_104018.1:n.550G>T
NM_000304.4:c.*41G>T MANE Select	NP_000295.1:n.*41G>T
NM_001281456.2:c.*41G>T	NP_001268385.1:n.*41G>T
NM_153321.3:c.*41G>T	NP_696996.1:n.*41G>T
NM_153322.3:c.*41G>T	NP_696997.1:n.*41G>T
NR_104017.2:n.619G>T
NR_104018.2:n.519G>T
NM_001281455.2:c.*41G>T	NP_001268384.1:n.*41G>T