Canonical Allele Identifier: CA1135959961

Linked Data

dbSNP Id: rs2074415036

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.103776905G>A , CM000685.2:g.103776905G>A GRCh38
NC_000023.10:g.103031833G>A , CM000685.1:g.103031833G>A GRCh37
NC_000023.9:g.102918489G>A NCBI36
NG_008863.2:g.5395G>A
NG_016452.2:g.60378C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000621218.5:c.-91G>A (PLP1) MANE Select ENSP00000484450.1:n.-91G>A
ENST00000422393.5:c.-91G>A (PLP1) ENSP00000413931.1:n.-91G>A
ENST00000433491.5:c.-91G>A (PLP1) ENSP00000393391.1:n.-91G>A
ENST00000434483.5:c.-91G>A (PLP1) ENSP00000403335.1:n.-91G>A
ENST00000443502.5:c.-91G>A (PLP1) ENSP00000391853.1:n.-91G>A
ENST00000455268.5:c.-91G>A (PLP1) ENSP00000409802.1:n.-91G>A
ENST00000464776.5:n.32G>A (PLP1)
ENST00000465975.1:n.32G>A (PLP1)
ENST00000494475.5:c.-91G>A (PLP1) ENSP00000480409.1:n.-91G>A
ENST00000612423.4:c.-91G>A (PLP1) ENSP00000481006.1:n.-91G>A
ENST00000619236.1:c.-91G>A (PLP1) ENSP00000477619.1:n.-91G>A
ENST00000619257.4:n.32G>A (PLP1)
ENST00000621218.4:c.-91G>A (PLP1) ENSP00000484450.1:n.-91G>A
NM_000533.4:c.-91G>A (PLP1) NP_000524.3:n.-91G>A
NM_001128834.2:c.-91G>A (PLP1) NP_001122306.1:n.-91G>A
NM_001305004.1:c.-91G>A (PLP1) NP_001291933.1:n.-91G>A
NM_199478.2:c.-91G>A (PLP1) NP_955772.1:n.-91G>A
XR_244483.3:n.863-252C>T
NR_146558.1:n.458-252C>T (RAB9B)
NR_146560.1:n.744-252C>T (RAB9B)
NM_000533.5:c.-91G>A (PLP1) MANE Select NP_000524.3:n.-91G>A
NM_199478.3:c.-91G>A (PLP1) NP_955772.1:n.-91G>A
NM_001128834.3:c.-91G>A (PLP1) NP_001122306.1:n.-91G>A
NR_146558.2:n.433-252C>T (RAB9B)
NR_146560.2:n.719-252C>T (RAB9B)