Canonical Allele Identifier: CA4087974

Gene: PLG

Linked Data

• dbSNP Id: rs773286811
• ExAC: 6:161162355 C / G
• gnomAD v2: 6-161162355-C-G
• gnomAD v4: 6-160741323-C-G
• MyVariant Identifiers: chr6:g.161162355C>G (hg19) ; chr6:g.160741323C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741323C>G , CM000668.2:g.160741323C>G	GRCh38
NC_000006.11:g.161162355C>G , CM000668.1:g.161162355C>G	GRCh37
NC_000006.10:g.161082345C>G	NCBI36
NG_016200.1:g.44131C>G , LRG_571:g.44131C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.984C>G	ENSP00000516619.1:p.Ile328Met
ENST00000418964.2:c.2082C>G	ENSP00000389424.2:p.Ile694Met
ENST00000706906.1:c.*2051C>G	ENSP00000516618.1:n.*2051C>G
ENST00000308192.14:c.2031C>G MANE Select	ENSP00000308938.9:p.Ile677Met
ENST00000308192.13:c.2031C>G	ENSP00000308938.9:p.Ile677Met
ENST00000461414.2:n.54C>G
ENST00000467466.1:n.332C>G
NM_000301.3:c.2031C>G , LRG_571t1:c.2031C>G	NP_000292.1:p.Ile677Met
NM_000301.4:c.2031C>G	NP_000292.1:p.Ile677Met
NM_000301.5:c.2031C>G MANE Select	NP_000292.1:p.Ile677Met