Canonical Allele Identifier: CA334001167

Linked Data

dbSNP Id: rs113951193

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.103786463A>G , CM000685.2:g.103786463A>G GRCh38
NC_000023.10:g.103041392A>G , CM000685.1:g.103041392A>G GRCh37
NC_000023.9:g.102928048A>G NCBI36
NG_008863.2:g.14953A>G
NG_016452.2:g.50820T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000621218.5:c.192-2A>G (PLP1) MANE Select ENSP00000484450.1:n.192-2A>G
ENST00000422393.5:c.192-2A>G (PLP1) ENSP00000413931.1:n.192-2A>G
ENST00000433491.5:c.192-2A>G (PLP1) ENSP00000393391.1:n.192-2A>G
ENST00000434483.5:c.192-2A>G (PLP1) ENSP00000403335.1:n.192-2A>G
ENST00000443502.5:c.192-2A>G (PLP1) ENSP00000391853.1:n.192-2A>G
ENST00000455268.5:c.192-2A>G (PLP1) ENSP00000409802.1:n.192-2A>G
ENST00000461231.5:n.108-2A>G (PLP1)
ENST00000464776.5:n.456-2A>G (PLP1)
ENST00000465975.1:n.312-264A>G (PLP1)
ENST00000476160.1:n.171-2A>G (PLP1)
ENST00000478642.5:n.173-2A>G (PLP1)
ENST00000479569.5:n.343-2A>G (PLP1)
ENST00000485688.5:n.34-2A>G (PLP1)
ENST00000485931.5:n.270-2A>G (PLP1)
ENST00000494475.5:c.192-2A>G (PLP1) ENSP00000480409.1:n.192-2A>G
ENST00000495678.5:n.494-2A>G (PLP1)
ENST00000612423.4:c.192-2A>G (PLP1) ENSP00000481006.1:n.192-2A>G
ENST00000619236.1:c.192-2A>G (PLP1) ENSP00000477619.1:n.192-2A>G
ENST00000619257.4:n.422-2A>G (PLP1)
ENST00000621218.4:c.192-2A>G (PLP1) ENSP00000484450.1:n.192-2A>G
NM_000533.4:c.192-2A>G (PLP1) NP_000524.3:n.192-2A>G
NM_001128834.2:c.192-2A>G (PLP1) NP_001122306.1:n.192-2A>G
NM_001305004.1:c.27-2A>G (PLP1) NP_001291933.1:n.27-2A>G
NM_199478.2:c.192-2A>G (PLP1) NP_955772.1:n.192-2A>G
XR_244483.3:n.862+6218T>C
NR_146558.1:n.457+6218T>C (RAB9B)
NR_146560.1:n.743+6218T>C (RAB9B)
NM_000533.5:c.192-2A>G (PLP1) MANE Select NP_000524.3:n.192-2A>G
NM_199478.3:c.192-2A>G (PLP1) NP_955772.1:n.192-2A>G
NM_001128834.3:c.192-2A>G (PLP1) NP_001122306.1:n.192-2A>G
NR_146558.2:n.432+6218T>C (RAB9B)
NR_146560.2:n.718+6218T>C (RAB9B)