Canonical Allele Identifier: CA4087778
Community Standard Title: NM_000301.5(PLG):c.1432G>A (p.Glu478Lys)
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160731226G>A , CM000668.2:g.160731226G>A GRCh38
NC_000006.11:g.161152258G>A , CM000668.1:g.161152258G>A GRCh37
NC_000006.10:g.161072248G>A NCBI36
NG_016200.1:g.34034G>A , LRG_571:g.34034G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000301.5:c.1432G>A MANE Select NP_000292.1:p.Glu478Lys
ENST00000308192.14:c.1432G>A MANE Select ENSP00000308938.9:p.Glu478Lys
NM_000301.3:c.1432G>A , LRG_571t1:c.1432G>A NP_000292.1:p.Glu478Lys
NM_000301.4:c.1432G>A NP_000292.1:p.Glu478Lys
ENST00000297289.8:n.430G>A
ENST00000297289.9:c.385G>A ENSP00000516619.1:p.Glu129Lys
ENST00000308192.13:c.1432G>A ENSP00000308938.9:p.Glu478Lys
ENST00000418964.2:c.1483G>A ENSP00000389424.2:p.Glu495Lys
ENST00000493435.1:n.487G>A
ENST00000706906.1:c.1432G>A ENSP00000516618.1:p.Glu478Lys