Canonical Allele Identifier: CA453029594

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161162406T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741374T>G , CM000668.2:g.160741374T>G	GRCh38
NC_000006.11:g.161162406T>G , CM000668.1:g.161162406T>G	GRCh37
NC_000006.10:g.161082396T>G	NCBI36
NG_016200.1:g.44182T>G , LRG_571:g.44182T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297289.9:c.1035T>G	ENSP00000516619.1:p.Ala345=
ENST00000418964.2:c.2133T>G	ENSP00000389424.2:p.Ala711=
ENST00000706906.1:c.*2102T>G	ENSP00000516618.1:n.*2102T>G
ENST00000308192.14:c.2082T>G MANE Select	ENSP00000308938.9:p.Ala694=
ENST00000308192.13:c.2082T>G	ENSP00000308938.9:p.Ala694=
ENST00000461414.2:n.99+6T>G
ENST00000467466.1:n.383T>G
NM_000301.3:c.2082T>G , LRG_571t1:c.2082T>G	NP_000292.1:p.Ala694=
NM_000301.4:c.2082T>G	NP_000292.1:p.Ala694=
NM_000301.5:c.2082T>G MANE Select	NP_000292.1:p.Ala694=