Canonical Allele Identifier: CA1677205987
Gene: PLG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.992A= ENSP00000516619.1:p.Lys331=
ENST00000418964.2:c.2090A= ENSP00000389424.2:p.Lys697=
ENST00000706906.1:c.*2059A= ENSP00000516618.1:n.*2059A=
ENST00000308192.14:c.2039A= MANE Select ENSP00000308938.9:p.Lys680=
ENST00000308192.13:c.2039A= ENSP00000308938.9:p.Lys680=
ENST00000461414.2:n.62A=
ENST00000467466.1:n.340A=
NM_000301.3:c.2039A= , LRG_571t1:c.2039A= NP_000292.1:p.Lys680=
NM_000301.4:c.2039A= NP_000292.1:p.Lys680=
NM_000301.5:c.2039A= MANE Select NP_000292.1:p.Lys680=