Canonical Allele Identifier: CA366366183

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161162357C>G (hg19) ; chr6:g.160741325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741325C>G , CM000668.2:g.160741325C>G	GRCh38
NC_000006.11:g.161162357C>G , CM000668.1:g.161162357C>G	GRCh37
NC_000006.10:g.161082347C>G	NCBI36
NG_016200.1:g.44133C>G , LRG_571:g.44133C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.986C>G	ENSP00000516619.1:p.Thr329Ser
ENST00000418964.2:c.2084C>G	ENSP00000389424.2:p.Thr695Ser
ENST00000706906.1:c.*2053C>G	ENSP00000516618.1:n.*2053C>G
ENST00000308192.14:c.2033C>G MANE Select	ENSP00000308938.9:p.Thr678Ser
ENST00000308192.13:c.2033C>G	ENSP00000308938.9:p.Thr678Ser
ENST00000461414.2:n.56C>G
ENST00000467466.1:n.334C>G
NM_000301.3:c.2033C>G , LRG_571t1:c.2033C>G	NP_000292.1:p.Thr678Ser
NM_000301.4:c.2033C>G	NP_000292.1:p.Thr678Ser
NM_000301.5:c.2033C>G MANE Select	NP_000292.1:p.Thr678Ser