Canonical Allele Identifier: CA334001175

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.103786727G>C , CM000685.2:g.103786727G>C GRCh38
NC_000023.10:g.103041656G>C , CM000685.1:g.103041656G>C GRCh37
NC_000023.9:g.102928312G>C NCBI36
NG_008863.2:g.15217G>C
NG_016452.2:g.50556C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000533.5:c.453+1G>C (PLP1) MANE Select NP_000524.3:n.453+1G>C
ENST00000621218.5:c.453+1G>C (PLP1) MANE Select ENSP00000484450.1:n.453+1G>C
NM_000533.4:c.453+1G>C (PLP1) NP_000524.3:n.453+1G>C
NM_001128834.2:c.453+1G>C (PLP1) NP_001122306.1:n.453+1G>C
NM_001128834.3:c.453+1G>C (PLP1) NP_001122306.1:n.453+1G>C
NM_001305004.1:c.288+1G>C (PLP1) NP_001291933.1:n.288+1G>C
NM_199478.2:c.348+106G>C (PLP1) NP_955772.1:n.348+106G>C
NM_199478.3:c.348+106G>C (PLP1) NP_955772.1:n.348+106G>C
NR_146558.1:n.457+5954C>G (RAB9B)
NR_146558.2:n.432+5954C>G (RAB9B)
NR_146560.1:n.743+5954C>G (RAB9B)
NR_146560.2:n.718+5954C>G (RAB9B)
ENST00000461231.5:n.264+106G>C (PLP1)
ENST00000465975.1:n.312G>C (PLP1)
ENST00000476160.1:n.433G>C (PLP1)
ENST00000478642.5:n.434+1G>C (PLP1)
ENST00000479569.5:n.499+106G>C (PLP1)
ENST00000485688.5:n.190+106G>C (PLP1)
ENST00000485931.5:n.532G>C (PLP1)
ENST00000612423.4:c.453+1G>C (PLP1) ENSP00000481006.1:n.453+1G>C
ENST00000619236.1:c.348+106G>C (PLP1) ENSP00000477619.1:n.348+106G>C
ENST00000621218.4:c.453+1G>C (PLP1) ENSP00000484450.1:n.453+1G>C
XR_244483.3:n.862+5954C>G