Canonical Allele Identifier: CA366366196

Gene: PLG

Linked Data

• gnomAD v4: 6-160741329-C-A
• MyVariant Identifiers: chr6:g.161162361C>A (hg19) ; chr6:g.160741329C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741329C>A , CM000668.2:g.160741329C>A	GRCh38
NC_000006.11:g.161162361C>A , CM000668.1:g.161162361C>A	GRCh37
NC_000006.10:g.161082351C>A	NCBI36
NG_016200.1:g.44137C>A , LRG_571:g.44137C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.990C>A	ENSP00000516619.1:p.Asp330Glu
ENST00000418964.2:c.2088C>A	ENSP00000389424.2:p.Asp696Glu
ENST00000706906.1:c.*2057C>A	ENSP00000516618.1:n.*2057C>A
ENST00000308192.14:c.2037C>A MANE Select	ENSP00000308938.9:p.Asp679Glu
ENST00000308192.13:c.2037C>A	ENSP00000308938.9:p.Asp679Glu
ENST00000461414.2:n.60C>A
ENST00000467466.1:n.338C>A
NM_000301.3:c.2037C>A , LRG_571t1:c.2037C>A	NP_000292.1:p.Asp679Glu
NM_000301.4:c.2037C>A	NP_000292.1:p.Asp679Glu
NM_000301.5:c.2037C>A MANE Select	NP_000292.1:p.Asp679Glu