Canonical Allele Identifier: CA366363862

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161152247A>T (hg19) ; chr6:g.160731215A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.374A>T	ENSP00000516619.1:p.Glu125Val
ENST00000418964.2:c.1472A>T	ENSP00000389424.2:p.Glu491Val
ENST00000706906.1:c.1421A>T	ENSP00000516618.1:p.Glu474Val
ENST00000308192.14:c.1421A>T MANE Select	ENSP00000308938.9:p.Glu474Val
ENST00000297289.8:n.419A>T
ENST00000308192.13:c.1421A>T	ENSP00000308938.9:p.Glu474Val
ENST00000493435.1:n.476A>T
NM_000301.3:c.1421A>T , LRG_571t1:c.1421A>T	NP_000292.1:p.Glu474Val
NM_000301.4:c.1421A>T	NP_000292.1:p.Glu474Val
NM_000301.5:c.1421A>T MANE Select	NP_000292.1:p.Glu474Val