Canonical Allele Identifier: CA1677201403
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160731229G= , CM000668.2:g.160731229G= GRCh38
NC_000006.11:g.161152261G= , CM000668.1:g.161152261G= GRCh37
NC_000006.10:g.161072251G= NCBI36
NG_016200.1:g.34037G= , LRG_571:g.34037G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297289.9:c.388G= ENSP00000516619.1:p.Glu130=
ENST00000418964.2:c.1486G= ENSP00000389424.2:p.Glu496=
ENST00000706906.1:c.1435G= ENSP00000516618.1:p.Glu479=
ENST00000308192.14:c.1435G= MANE Select ENSP00000308938.9:p.Glu479=
ENST00000297289.8:n.433G=
ENST00000308192.13:c.1435G= ENSP00000308938.9:p.Glu479=
ENST00000493435.1:n.490G=
NM_000301.3:c.1435G= , LRG_571t1:c.1435G= NP_000292.1:p.Glu479=
NM_000301.4:c.1435G= NP_000292.1:p.Glu479=
NM_000301.5:c.1435G= MANE Select NP_000292.1:p.Glu479=