Canonical Allele Identifier: CA398268285

Gene: PMP22

Linked Data

• ClinVar Variation Id: 637834
• ClinVar RCV Id: RCV000790164
• dbSNP Id: rs104894620
• MyVariant Identifiers: chr17:g.15142901A>C (hg19) ; chr17:g.15239584A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15239584A>C , CM000679.2:g.15239584A>C	GRCh38
NC_000017.10:g.15142901A>C , CM000679.1:g.15142901A>C	GRCh37
NC_000017.9:g.15083626A>C	NCBI36
NG_007949.1:g.30744T>G , LRG_263:g.30744T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.206T>G MANE Select	ENSP00000308937.3:p.Met69Arg
ENST00000395936.7:c.206T>G	ENSP00000379268.1:p.Met69Arg
ENST00000395938.7:c.195T>G	ENSP00000379269.3:p.His65Gln
ENST00000426385.4:c.206T>G	ENSP00000409824.3:p.Met69Arg
ENST00000494511.7:c.2T>G	ENSP00000462782.2:p.Met1Arg
ENST00000580584.3:c.2T>G	ENSP00000464468.3:p.Met1Arg
ENST00000612492.5:c.206T>G	ENSP00000484631.1:p.Met69Arg
ENST00000643451.2:c.206T>G	ENSP00000494628.1:p.Met69Arg
ENST00000644020.1:c.206T>G	ENSP00000496522.1:p.Met69Arg
ENST00000646419.2:c.206T>G	ENSP00000494871.1:p.Met69Arg
ENST00000674651.1:c.206T>G	ENSP00000501727.1:p.Met69Arg
ENST00000674673.1:c.206T>G	ENSP00000501804.1:p.Met69Arg
ENST00000674707.1:c.2T>G	ENSP00000502250.1:p.Met1Arg
ENST00000674868.1:c.206T>G	ENSP00000502835.1:p.Met69Arg
ENST00000674871.1:n.222T>G
ENST00000674947.1:c.195T>G	ENSP00000501580.1:p.His65Gln
ENST00000675197.1:n.186T>G
ENST00000675350.1:c.206T>G	ENSP00000501557.1:p.Met69Arg
ENST00000675551.1:c.206T>G	ENSP00000501945.1:p.Met69Arg
ENST00000675808.1:c.206T>G	ENSP00000502310.1:p.Met69Arg
ENST00000675819.1:c.206T>G	ENSP00000502018.1:p.Met69Arg
ENST00000675854.1:c.2T>G	ENSP00000502324.1:p.Met1Arg
ENST00000675950.1:c.206T>G	ENSP00000501546.1:p.Met69Arg
ENST00000676161.1:c.179-8504T>G	ENSP00000501766.1:n.179-8504T>G
ENST00000676221.1:c.206T>G	ENSP00000502601.1:p.Met69Arg
ENST00000676329.1:c.308T>G	ENSP00000501698.1:p.Met103Arg
ENST00000312280.7:c.206T>G	ENSP00000308937.3:p.Met69Arg
ENST00000395936.5:c.206T>G	ENSP00000379268.1:p.Met69Arg
ENST00000395938.6:c.206T>G	ENSP00000379269.2:p.Met69Arg
ENST00000426385.3:c.206T>G	ENSP00000409824.3:p.Met69Arg
ENST00000494511.5:c.27T>G	ENSP00000462782.1:p.His9Gln
ENST00000580584.1:c.27T>G	ENSP00000464468.1:p.His9Gln
ENST00000612492.4:c.206T>G	ENSP00000484631.1:p.Met69Arg
NM_000304.3:c.206T>G	NP_000295.1:p.Met69Arg
NM_001281455.1:c.206T>G	NP_001268384.1:p.Met69Arg
NM_001281456.1:c.206T>G	NP_001268385.1:p.Met69Arg
NM_153321.2:c.206T>G	NP_696996.1:p.Met69Arg
NM_153322.2:c.206T>G	NP_696997.1:p.Met69Arg
NR_104017.1:n.332T>G
NR_104018.1:n.232T>G
XM_011523943.1:c.206T>G	XP_011522245.1:p.Met69Arg
NM_001330143.1:c.206T>G	NP_001317072.1:p.Met69Arg
XM_024450806.1:c.206T>G	XP_024306574.1:p.Met69Arg
NM_000304.4:c.206T>G MANE Select	NP_000295.1:p.Met69Arg
NM_001281456.2:c.206T>G	NP_001268385.1:p.Met69Arg
NM_001330143.2:c.206T>G	NP_001317072.1:p.Met69Arg
NM_153321.3:c.206T>G	NP_696996.1:p.Met69Arg
NM_153322.3:c.206T>G	NP_696997.1:p.Met69Arg
NR_104017.2:n.301T>G
NR_104018.2:n.201T>G
NM_001281455.2:c.206T>G	NP_001268384.1:p.Met69Arg