Canonical Allele Identifier: CA453029362

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161162352C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741320C>T , CM000668.2:g.160741320C>T	GRCh38
NC_000006.11:g.161162352C>T , CM000668.1:g.161162352C>T	GRCh37
NC_000006.10:g.161082342C>T	NCBI36
NG_016200.1:g.44128C>T , LRG_571:g.44128C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.981C>T	ENSP00000516619.1:p.Val327=
ENST00000418964.2:c.2079C>T	ENSP00000389424.2:p.Val693=
ENST00000706906.1:c.*2048C>T	ENSP00000516618.1:n.*2048C>T
ENST00000308192.14:c.2028C>T MANE Select	ENSP00000308938.9:p.Val676=
ENST00000308192.13:c.2028C>T	ENSP00000308938.9:p.Val676=
ENST00000461414.2:n.51C>T
ENST00000467466.1:n.329C>T
NM_000301.3:c.2028C>T , LRG_571t1:c.2028C>T	NP_000292.1:p.Val676=
NM_000301.4:c.2028C>T	NP_000292.1:p.Val676=
NM_000301.5:c.2028C>T MANE Select	NP_000292.1:p.Val676=