Canonical Allele Identifier: CA366363866

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161152249A>G (hg19) ; chr6:g.160731217A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160731217A>G , CM000668.2:g.160731217A>G	GRCh38
NC_000006.11:g.161152249A>G , CM000668.1:g.161152249A>G	GRCh37
NC_000006.10:g.161072239A>G	NCBI36
NG_016200.1:g.34025A>G , LRG_571:g.34025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.376A>G	ENSP00000516619.1:p.Thr126Ala
ENST00000418964.2:c.1474A>G	ENSP00000389424.2:p.Thr492Ala
ENST00000706906.1:c.1423A>G	ENSP00000516618.1:p.Thr475Ala
ENST00000308192.14:c.1423A>G MANE Select	ENSP00000308938.9:p.Thr475Ala
ENST00000297289.8:n.421A>G
ENST00000308192.13:c.1423A>G	ENSP00000308938.9:p.Thr475Ala
ENST00000493435.1:n.478A>G
NM_000301.3:c.1423A>G , LRG_571t1:c.1423A>G	NP_000292.1:p.Thr475Ala
NM_000301.4:c.1423A>G	NP_000292.1:p.Thr475Ala
NM_000301.5:c.1423A>G MANE Select	NP_000292.1:p.Thr475Ala