Canonical Allele Identifier: CA2449052802

Gene: PLP1 RAB9B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.103785799_103785800delinsCT , CM000685.2:g.103785799_103785800delinsCT	GRCh38
NC_000023.10:g.103040728_103040729delinsCT , CM000685.1:g.103040728_103040729delinsCT	GRCh37
NC_000023.9:g.102927384_102927385delinsCT	NCBI36
NG_008863.2:g.14289_14290delinsCT
NG_016452.2:g.51483_51484delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621218.5:c.191+31_191+32delinsCT (PLP1) MANE Select	ENSP00000484450.1:n.191+31_191+32delinsCT
ENST00000422393.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000413931.1:n.191+31_191+32delinsCT
ENST00000433491.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000393391.1:n.191+31_191+32delinsCT
ENST00000434483.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000403335.1:n.191+31_191+32delinsCT
ENST00000443502.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000391853.1:n.191+31_191+32delinsCT
ENST00000455268.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000409802.1:n.191+31_191+32delinsCT
ENST00000464776.5:n.455+31_455+32delinsCT (PLP1)
ENST00000465975.1:n.311+33_311+34delinsCT (PLP1)
ENST00000479569.5:n.342+31_342+32delinsCT (PLP1)
ENST00000480325.1:n.301_302delinsCT (PLP1)
ENST00000485931.5:n.269+31_269+32delinsCT (PLP1)
ENST00000494475.5:c.191+31_191+32delinsCT (PLP1)	ENSP00000480409.1:n.191+31_191+32delinsCT
ENST00000495678.5:n.493+31_493+32delinsCT (PLP1)
ENST00000612423.4:c.191+31_191+32delinsCT (PLP1)	ENSP00000481006.1:n.191+31_191+32delinsCT
ENST00000619236.1:c.191+31_191+32delinsCT (PLP1)	ENSP00000477619.1:n.191+31_191+32delinsCT
ENST00000619257.4:n.421+31_421+32delinsCT (PLP1)
ENST00000621218.4:c.191+31_191+32delinsCT (PLP1)	ENSP00000484450.1:n.191+31_191+32delinsCT
NM_000533.4:c.191+31_191+32delinsCT (PLP1)	NP_000524.3:n.191+31_191+32delinsCT
NM_001128834.2:c.191+31_191+32delinsCT (PLP1)	NP_001122306.1:n.191+31_191+32delinsCT
NM_001305004.1:c.26+31_26+32delinsCT (PLP1)	NP_001291933.1:n.26+31_26+32delinsCT
NM_199478.2:c.191+31_191+32delinsCT (PLP1)	NP_955772.1:n.191+31_191+32delinsCT
XR_244483.3:n.862+6881_862+6882delinsAG
NR_146558.1:n.457+6881_457+6882delinsAG (RAB9B)
NR_146560.1:n.743+6881_743+6882delinsAG (RAB9B)
NM_000533.5:c.191+31_191+32delinsCT (PLP1) MANE Select	NP_000524.3:n.191+31_191+32delinsCT
NM_199478.3:c.191+31_191+32delinsCT (PLP1)	NP_955772.1:n.191+31_191+32delinsCT
NM_001128834.3:c.191+31_191+32delinsCT (PLP1)	NP_001122306.1:n.191+31_191+32delinsCT
NR_146558.2:n.432+6881_432+6882delinsAG (RAB9B)
NR_146560.2:n.718+6881_718+6882delinsAG (RAB9B)