Canonical Allele Identifier: CA366363760
Community Standard Title: NM_000301.5(PLG):c.1366G>C (p.Gly456Arg)
Gene: PLG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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