Canonical Allele Identifier: CA366363868

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161152250C>A (hg19) ; chr6:g.160731218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160731218C>A , CM000668.2:g.160731218C>A	GRCh38
NC_000006.11:g.161152250C>A , CM000668.1:g.161152250C>A	GRCh37
NC_000006.10:g.161072240C>A	NCBI36
NG_016200.1:g.34026C>A , LRG_571:g.34026C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.377C>A	ENSP00000516619.1:p.Thr126Asn
ENST00000418964.2:c.1475C>A	ENSP00000389424.2:p.Thr492Asn
ENST00000706906.1:c.1424C>A	ENSP00000516618.1:p.Thr475Asn
ENST00000308192.14:c.1424C>A MANE Select	ENSP00000308938.9:p.Thr475Asn
ENST00000297289.8:n.422C>A
ENST00000308192.13:c.1424C>A	ENSP00000308938.9:p.Thr475Asn
ENST00000493435.1:n.479C>A
NM_000301.3:c.1424C>A , LRG_571t1:c.1424C>A	NP_000292.1:p.Thr475Asn
NM_000301.4:c.1424C>A	NP_000292.1:p.Thr475Asn
NM_000301.5:c.1424C>A MANE Select	NP_000292.1:p.Thr475Asn