Canonical Allele Identifier: CA366363759
Community Standard Title: NM_000301.5(PLG):c.1366G>A (p.Gly456Arg)
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160731160G>A , CM000668.2:g.160731160G>A GRCh38
NC_000006.11:g.161152192G>A , CM000668.1:g.161152192G>A GRCh37
NC_000006.10:g.161072182G>A NCBI36
NG_016200.1:g.33968G>A , LRG_571:g.33968G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000301.5:c.1366G>A MANE Select NP_000292.1:p.Gly456Arg
ENST00000308192.14:c.1366G>A MANE Select ENSP00000308938.9:p.Gly456Arg
NM_000301.3:c.1366G>A , LRG_571t1:c.1366G>A NP_000292.1:p.Gly456Arg
NM_000301.4:c.1366G>A NP_000292.1:p.Gly456Arg
ENST00000297289.8:n.364G>A
ENST00000297289.9:c.319G>A ENSP00000516619.1:p.Gly107Arg
ENST00000308192.13:c.1366G>A ENSP00000308938.9:p.Gly456Arg
ENST00000418964.2:c.1417G>A ENSP00000389424.2:p.Gly473Arg
ENST00000493435.1:n.421G>A
ENST00000706906.1:c.1366G>A ENSP00000516618.1:p.Gly456Arg