Canonical Allele Identifier: CA398739670

Gene: PMP22

Linked Data

• MyVariant Identifiers: chr17:g.15134332C>G (hg19) ; chr17:g.15231015C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15231015C>G , CM000679.2:g.15231015C>G	GRCh38
NC_000017.10:g.15134332C>G , CM000679.1:g.15134332C>G	GRCh37
NC_000017.9:g.15075057C>G	NCBI36
NG_007949.1:g.39313G>C , LRG_263:g.39313G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312280.9:c.385G>C MANE Select	ENSP00000308937.3:p.Asp129His
ENST00000395936.7:c.*94G>C	ENSP00000379268.1:n.*94G>C
ENST00000395938.7:c.374G>C	ENSP00000379269.3:p.Gly125Ala
ENST00000494511.7:c.181G>C	ENSP00000462782.2:p.Asp61His
ENST00000580584.3:c.181G>C	ENSP00000464468.3:p.Asp61His
ENST00000612492.5:c.385G>C	ENSP00000484631.1:p.Asp129His
ENST00000643451.2:c.*240G>C	ENSP00000494628.1:n.*240G>C
ENST00000644020.1:c.*94G>C	ENSP00000496522.1:n.*94G>C
ENST00000646419.2:c.*94G>C	ENSP00000494871.1:n.*94G>C
ENST00000674651.1:c.385G>C	ENSP00000501727.1:p.Asp129His
ENST00000674673.1:c.385G>C	ENSP00000501804.1:p.Asp129His
ENST00000674707.1:c.181G>C	ENSP00000502250.1:p.Asp61His
ENST00000674868.1:c.385G>C	ENSP00000502835.1:p.Asp129His
ENST00000674871.1:n.401G>C
ENST00000674947.1:c.374G>C	ENSP00000501580.1:p.Gly125Ala
ENST00000675197.1:n.365G>C
ENST00000675350.1:c.385G>C	ENSP00000501557.1:p.Asp129His
ENST00000675551.1:c.*54G>C	ENSP00000501945.1:n.*54G>C
ENST00000675808.1:c.385G>C	ENSP00000502310.1:p.Asp129His
ENST00000675819.1:c.385G>C	ENSP00000502018.1:p.Asp129His
ENST00000675854.1:c.181G>C	ENSP00000502324.1:p.Asp61His
ENST00000675950.1:c.385G>C	ENSP00000501546.1:p.Asp129His
ENST00000676002.1:n.378G>C
ENST00000676161.1:c.244G>C	ENSP00000501766.1:p.Asp82His
ENST00000676221.1:c.385G>C	ENSP00000502601.1:p.Asp129His
ENST00000676329.1:c.487G>C	ENSP00000501698.1:p.Asp163His
ENST00000312280.7:c.385G>C	ENSP00000308937.3:p.Asp129His
ENST00000395936.5:c.*94G>C	ENSP00000379268.1:n.*94G>C
ENST00000395938.6:c.385G>C	ENSP00000379269.2:p.Asp129His
ENST00000494511.5:c.206G>C	ENSP00000462782.1:p.Gly69Ala
ENST00000612492.4:c.385G>C	ENSP00000484631.1:p.Asp129His
NM_000304.3:c.385G>C	NP_000295.1:p.Asp129His
NM_001281455.1:c.385G>C	NP_001268384.1:p.Asp129His
NM_001281456.1:c.385G>C	NP_001268385.1:p.Asp129His
NM_153321.2:c.385G>C	NP_696996.1:p.Asp129His
NM_153322.2:c.385G>C	NP_696997.1:p.Asp129His
NR_104017.1:n.511G>C
NR_104018.1:n.411G>C
NM_000304.4:c.385G>C MANE Select	NP_000295.1:p.Asp129His
NM_001281456.2:c.385G>C	NP_001268385.1:p.Asp129His
NM_153321.3:c.385G>C	NP_696996.1:p.Asp129His
NM_153322.3:c.385G>C	NP_696997.1:p.Asp129His
NR_104017.2:n.480G>C
NR_104018.2:n.380G>C
NM_001281455.2:c.385G>C	NP_001268384.1:p.Asp129His