Canonical Allele Identifier: CA366362675
Community Standard Title: NM_000301.5(PLG):c.886T>G (p.Cys296Gly)
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160718392T>G , CM000668.2:g.160718392T>G GRCh38
NC_000006.11:g.161139424T>G , CM000668.1:g.161139424T>G GRCh37
NC_000006.10:g.161059414T>G NCBI36
NG_016200.1:g.21200T>G , LRG_571:g.21200T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000301.5:c.886T>G MANE Select NP_000292.1:p.Cys296Gly
ENST00000308192.14:c.886T>G MANE Select ENSP00000308938.9:p.Cys296Gly
NM_000301.3:c.886T>G , LRG_571t1:c.886T>G NP_000292.1:p.Cys296Gly
NM_000301.4:c.886T>G NP_000292.1:p.Cys296Gly
ENST00000297289.8:n.95-4016T>G
ENST00000297289.9:c.50-4016T>G ENSP00000516619.1:n.50-4016T>G
ENST00000308192.13:c.886T>G ENSP00000308938.9:p.Cys296Gly
ENST00000418964.2:c.937T>G ENSP00000389424.2:p.Cys313Gly
ENST00000706906.1:c.886T>G ENSP00000516618.1:p.Cys296Gly