Canonical Allele Identifier: CA1096557201
Gene: PLG HGNC NCBI

Linked Data

dbSNP Id: rs553207544

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160741227G>A , CM000668.2:g.160741227G>A GRCh38
NC_000006.11:g.161162259G>A , CM000668.1:g.161162259G>A GRCh37
NC_000006.10:g.161082249G>A NCBI36
NG_016200.1:g.44035G>A , LRG_571:g.44035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297289.9:c.972-84G>A ENSP00000516619.1:n.972-84G>A
ENST00000418964.2:c.2070-84G>A ENSP00000389424.2:n.2070-84G>A
ENST00000706906.1:c.*2039-84G>A ENSP00000516618.1:n.*2039-84G>A
ENST00000308192.14:c.2019-84G>A MANE Select ENSP00000308938.9:n.2019-84G>A
ENST00000308192.13:c.2019-84G>A ENSP00000308938.9:n.2019-84G>A
ENST00000461414.2:n.42-84G>A
ENST00000467466.1:n.320-84G>A
NM_000301.3:c.2019-84G>A , LRG_571t1:c.2019-84G>A NP_000292.1:n.2019-84G>A
NM_000301.4:c.2019-84G>A NP_000292.1:n.2019-84G>A
NM_000301.5:c.2019-84G>A MANE Select NP_000292.1:n.2019-84G>A