Canonical Allele Identifier: CA1677195116

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160716958G= , CM000668.2:g.160716958G=	GRCh38
NC_000006.11:g.161137990G= , CM000668.1:g.161137990G=	GRCh37
NC_000006.10:g.161057980G=	NCBI36
NG_016200.1:g.19766G= , LRG_571:g.19766G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297289.9:c.50-5450G=	ENSP00000516619.1:n.50-5450G=
ENST00000418964.2:c.838+195G=	ENSP00000389424.2:n.838+195G=
ENST00000706906.1:c.787+195G=	ENSP00000516618.1:n.787+195G=
ENST00000308192.14:c.787+195G= MANE Select	ENSP00000308938.9:n.787+195G=
ENST00000297289.8:n.95-5450G=
ENST00000308192.13:c.787+195G=	ENSP00000308938.9:n.787+195G=
NM_000301.3:c.787+195G= , LRG_571t1:c.787+195G=	NP_000292.1:n.787+195G=
NM_000301.4:c.787+195G=	NP_000292.1:n.787+195G=
NM_000301.5:c.787+195G= MANE Select	NP_000292.1:n.787+195G=