Canonical Allele Identifier: CA1168598870
Gene: PLPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500739_56500743delinsTCACG , CM000663.2:g.56500739_56500743delinsTCACG GRCh38
NC_000001.10:g.56966411_56966415delinsTCACG , CM000663.1:g.56966411_56966415delinsTCACG GRCh37
NC_000001.9:g.56738999_56739003delinsTCACG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4067_811-4063delinsCGTGA MANE Select ENSP00000360296.3:n.811-4067_811-4063delinsCGTGA
ENST00000641109.1:c.220-4067_220-4063delinsCGTGA ENSP00000493138.1:n.220-4067_220-4063delinsCGTGA
ENST00000641494.1:c.65-4067_65-4063delinsCGTGA
ENST00000642129.1:c.455-4067_455-4063delinsCGTGA
ENST00000371250.3:c.811-4067_811-4063delinsCGTGA ENSP00000360296.3:n.811-4067_811-4063delinsCGTGA
ENST00000459962.1:n.1797-4067_1797-4063delinsCGTGA
ENST00000472957.1:n.296-4067_296-4063delinsCGTGA
NM_003713.4:c.811-4067_811-4063delinsCGTGA NP_003704.3:n.811-4067_811-4063delinsCGTGA
NM_003713.5:c.811-4067_811-4063delinsCGTGA MANE Select NP_003704.3:n.811-4067_811-4063delinsCGTGA