Canonical Allele Identifier: CA1677205986

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741328A= , CM000668.2:g.160741328A=	GRCh38
NC_000006.11:g.161162360A= , CM000668.1:g.161162360A=	GRCh37
NC_000006.10:g.161082350A=	NCBI36
NG_016200.1:g.44136A= , LRG_571:g.44136A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.989A=	ENSP00000516619.1:p.Asp330=
ENST00000418964.2:c.2087A=	ENSP00000389424.2:p.Asp696=
ENST00000706906.1:c.*2056A=	ENSP00000516618.1:n.*2056A=
ENST00000308192.14:c.2036A= MANE Select	ENSP00000308938.9:p.Asp679=
ENST00000308192.13:c.2036A=	ENSP00000308938.9:p.Asp679=
ENST00000461414.2:n.59A=
ENST00000467466.1:n.337A=
NM_000301.3:c.2036A= , LRG_571t1:c.2036A=	NP_000292.1:p.Asp679=
NM_000301.4:c.2036A=	NP_000292.1:p.Asp679=
NM_000301.5:c.2036A= MANE Select	NP_000292.1:p.Asp679=