Canonical Allele Identifier: CA375550958
Gene: PMPCA HGNC NCBI

Linked Data

dbSNP Id: rs778283114

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136410738A>G , CM000671.2:g.136410738A>G GRCh38
NC_000009.11:g.139305190A>G , CM000671.1:g.139305190A>G GRCh37
NC_000009.10:g.138425011A>G NCBI36
NG_046789.1:g.5166A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000444897.3:c.70A>G ENSP00000408393.2:p.Arg24Gly
ENST00000612553.5:n.98A>G
ENST00000706227.1:c.70A>G ENSP00000516285.1:p.Arg24Gly
ENST00000706228.1:c.70A>G ENSP00000516286.1:p.Arg24Gly
ENST00000706375.1:c.70A>G ENSP00000516357.1:p.Arg24Gly
ENST00000706376.1:c.70A>G ENSP00000516358.1:p.Arg24Gly
ENST00000706377.1:c.70A>G ENSP00000516359.1:p.Arg24Gly
ENST00000706378.1:n.98A>G
ENST00000706379.1:c.70A>G ENSP00000516360.1:p.Arg24Gly
ENST00000706380.1:c.70A>G ENSP00000516361.1:p.Arg24Gly
ENST00000706381.1:n.95A>G
ENST00000706382.1:n.95A>G
ENST00000706383.1:n.95A>G
ENST00000706384.1:c.70A>G ENSP00000516362.1:p.Arg24Gly
ENST00000706385.1:c.70A>G ENSP00000516363.1:p.Arg24Gly
ENST00000706386.1:c.70A>G ENSP00000516364.1:p.Arg24Gly
ENST00000706387.1:c.70A>G ENSP00000516365.1:p.Arg24Gly
ENST00000706388.1:c.70A>G ENSP00000516366.1:p.Arg24Gly
ENST00000706389.1:n.85A>G
ENST00000706390.1:c.70A>G ENSP00000516367.1:p.Arg24Gly
ENST00000371717.8:c.70A>G MANE Select ENSP00000360782.3:p.Arg24Gly
ENST00000371717.7:c.70A>G ENSP00000360782.3:p.Arg24Gly
ENST00000371720.5:n.81A>G
ENST00000399219.7:c.-229A>G ENSP00000416702.2:n.-229A>G
ENST00000612553.4:n.98A>G
ENST00000614402.4:n.65A>G
ENST00000619192.4:n.95A>G
ENST00000620412.4:n.81A>G
ENST00000622209.4:n.79A>G
NM_001282944.1:c.-229A>G NP_001269873.1:n.-229A>G
NM_001282946.1:c.-229A>G NP_001269875.1:n.-229A>G
NM_015160.2:c.70A>G NP_055975.1:p.Arg24Gly
XM_005266059.3:c.70A>G XP_005266116.1:p.Arg24Gly
XM_005266059.4:c.70A>G XP_005266116.1:p.Arg24Gly
XM_017014543.2:c.-505A>G XP_016870032.1:n.-505A>G
NM_015160.3:c.70A>G MANE Select NP_055975.1:p.Arg24Gly
NM_001282944.2:c.-229A>G NP_001269873.1:n.-229A>G
NM_001282946.2:c.-229A>G NP_001269875.1:n.-229A>G