Canonical Allele Identifier: CA1677196039

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160722576T= , CM000668.2:g.160722576T=	GRCh38
NC_000006.11:g.161143608T= , CM000668.1:g.161143608T=	GRCh37
NC_000006.10:g.161063598T=	NCBI36
NG_016200.1:g.25384T= , LRG_571:g.25384T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297289.9:c.209+9T=	ENSP00000516619.1:n.209+9T=
ENST00000418964.2:c.1307+9T=	ENSP00000389424.2:n.1307+9T=
ENST00000706906.1:c.1256+9T=	ENSP00000516618.1:n.1256+9T=
ENST00000308192.14:c.1256+9T= MANE Select	ENSP00000308938.9:n.1256+9T=
ENST00000297289.8:n.254+9T=
ENST00000308192.13:c.1256+9T=	ENSP00000308938.9:n.1256+9T=
NM_000301.3:c.1256+9T= , LRG_571t1:c.1256+9T=	NP_000292.1:n.1256+9T=
NM_000301.4:c.1256+9T=	NP_000292.1:n.1256+9T=
NM_000301.5:c.1256+9T= MANE Select	NP_000292.1:n.1256+9T=