Canonical Allele Identifier: CA1677205985
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160741327G= , CM000668.2:g.160741327G= GRCh38
NC_000006.11:g.161162359G= , CM000668.1:g.161162359G= GRCh37
NC_000006.10:g.161082349G= NCBI36
NG_016200.1:g.44135G= , LRG_571:g.44135G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.988G= ENSP00000516619.1:p.Asp330=
ENST00000418964.2:c.2086G= ENSP00000389424.2:p.Asp696=
ENST00000706906.1:c.*2055G= ENSP00000516618.1:n.*2055G=
ENST00000308192.14:c.2035G= MANE Select ENSP00000308938.9:p.Asp679=
ENST00000308192.13:c.2035G= ENSP00000308938.9:p.Asp679=
ENST00000461414.2:n.58G=
ENST00000467466.1:n.336G=
NM_000301.3:c.2035G= , LRG_571t1:c.2035G= NP_000292.1:p.Asp679=
NM_000301.4:c.2035G= NP_000292.1:p.Asp679=
NM_000301.5:c.2035G= MANE Select NP_000292.1:p.Asp679=