Canonical Allele Identifier: CA366363861

Gene: PLG

Linked Data

• dbSNP Id: rs1228035650
• gnomAD v2: 6-161152247-A-G
• gnomAD v4: 6-160731215-A-G
• MyVariant Identifiers: chr6:g.161152247A>G (hg19) ; chr6:g.160731215A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160731215A>G , CM000668.2:g.160731215A>G	GRCh38
NC_000006.11:g.161152247A>G , CM000668.1:g.161152247A>G	GRCh37
NC_000006.10:g.161072237A>G	NCBI36
NG_016200.1:g.34023A>G , LRG_571:g.34023A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.374A>G	ENSP00000516619.1:p.Glu125Gly
ENST00000418964.2:c.1472A>G	ENSP00000389424.2:p.Glu491Gly
ENST00000706906.1:c.1421A>G	ENSP00000516618.1:p.Glu474Gly
ENST00000308192.14:c.1421A>G MANE Select	ENSP00000308938.9:p.Glu474Gly
ENST00000297289.8:n.419A>G
ENST00000308192.13:c.1421A>G	ENSP00000308938.9:p.Glu474Gly
ENST00000493435.1:n.476A>G
NM_000301.3:c.1421A>G , LRG_571t1:c.1421A>G	NP_000292.1:p.Glu474Gly
NM_000301.4:c.1421A>G	NP_000292.1:p.Glu474Gly
NM_000301.5:c.1421A>G MANE Select	NP_000292.1:p.Glu474Gly