Canonical Allele Identifier: CA366366212
Gene: PLG HGNC NCBI

Linked Data

dbSNP Id: rs1778190087

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160741331A>G , CM000668.2:g.160741331A>G GRCh38
NC_000006.11:g.161162363A>G , CM000668.1:g.161162363A>G GRCh37
NC_000006.10:g.161082353A>G NCBI36
NG_016200.1:g.44139A>G , LRG_571:g.44139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.992A>G ENSP00000516619.1:p.Lys331Arg
ENST00000418964.2:c.2090A>G ENSP00000389424.2:p.Lys697Arg
ENST00000706906.1:c.*2059A>G ENSP00000516618.1:n.*2059A>G
ENST00000308192.14:c.2039A>G MANE Select ENSP00000308938.9:p.Lys680Arg
ENST00000308192.13:c.2039A>G ENSP00000308938.9:p.Lys680Arg
ENST00000461414.2:n.62A>G
ENST00000467466.1:n.340A>G
NM_000301.3:c.2039A>G , LRG_571t1:c.2039A>G NP_000292.1:p.Lys680Arg
NM_000301.4:c.2039A>G NP_000292.1:p.Lys680Arg
NM_000301.5:c.2039A>G MANE Select NP_000292.1:p.Lys680Arg