Canonical Allele Identifier: CA1677189994

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160706469A= , CM000668.2:g.160706469A=	GRCh38
NC_000006.11:g.161127501A= , CM000668.1:g.161127501A=	GRCh37
NC_000006.10:g.161047491A=	NCBI36
NG_016200.1:g.9277A= , LRG_571:g.9277A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297289.9:c.49+4116A=	ENSP00000516619.1:n.49+4116A=
ENST00000418964.2:c.112A=	ENSP00000389424.2:p.Lys38=
ENST00000494325.2:c.-114A=	ENSP00000516620.1:n.-114A=
ENST00000706906.1:c.112A=	ENSP00000516618.1:p.Lys38=
ENST00000308192.14:c.112A= MANE Select	ENSP00000308938.9:p.Lys38=
ENST00000297289.8:n.94+4116A=
ENST00000308192.13:c.112A=	ENSP00000308938.9:p.Lys38=
ENST00000366924.6:c.112A=	ENSP00000355891.2:p.Lys38=
ENST00000418964.1:c.112A=	ENSP00000389424.1:p.Lys38=
ENST00000462918.5:n.149A=
ENST00000471691.1:n.95A=
ENST00000483038.5:n.125A=
ENST00000484367.5:n.1082A=
ENST00000494325.1:n.96A=
NM_000301.3:c.112A= , LRG_571t1:c.112A=	NP_000292.1:p.Lys38=
NM_001168338.1:c.112A= , LRG_571t2:c.112A=	NP_001161810.1:p.Lys38=
NM_000301.4:c.112A=	NP_000292.1:p.Lys38=
NM_000301.5:c.112A= MANE Select	NP_000292.1:p.Lys38=