Canonical Allele Identifier: CA2449049823

Gene: PLP1 RAB9B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.103776819T= , CM000685.2:g.103776819T=	GRCh38
NC_000023.10:g.103031747T= , CM000685.1:g.103031747T=	GRCh37
NC_000023.9:g.102918403T=	NCBI36
NG_008863.2:g.5309T=
NG_016452.2:g.60464A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422393.5:c.-143-34T= (PLP1)	ENSP00000413931.1:n.-143-34T=
ENST00000433491.5:c.-143-34T= (PLP1)	ENSP00000393391.1:n.-143-34T=
ENST00000434483.5:c.-143-34T= (PLP1)	ENSP00000403335.1:n.-143-34T=
ENST00000443502.5:c.-143-34T= (PLP1)	ENSP00000391853.1:n.-143-34T=
ENST00000455268.5:c.-143-34T= (PLP1)	ENSP00000409802.1:n.-143-34T=
ENST00000494475.5:c.-143-34T= (PLP1)	ENSP00000480409.1:n.-143-34T=
ENST00000612423.4:c.-143-34T= (PLP1)	ENSP00000481006.1:n.-143-34T=
NM_000533.4:c.-177T= (PLP1)	NP_000524.3:n.-177T=
NM_001128834.2:c.-143-34T= (PLP1)	NP_001122306.1:n.-143-34T=
NM_199478.2:c.-177T= (PLP1)	NP_955772.1:n.-177T=
XR_244483.3:n.863-166A=
NR_146558.1:n.458-166A= (RAB9B)
NR_146560.1:n.744-166A= (RAB9B)
NM_001128834.3:c.-143-34T= (PLP1)	NP_001122306.1:n.-143-34T=
NR_146558.2:n.433-166A= (RAB9B)
NR_146560.2:n.719-166A= (RAB9B)