Canonical Allele Identifier: CA1677206031

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741424T= , CM000668.2:g.160741424T=	GRCh38
NC_000006.11:g.161162456T= , CM000668.1:g.161162456T=	GRCh37
NC_000006.10:g.161082446T=	NCBI36
NG_016200.1:g.44232T= , LRG_571:g.44232T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+7T=	ENSP00000516619.1:n.1078+7T=
ENST00000418964.2:c.2176+7T=	ENSP00000389424.2:n.2176+7T=
ENST00000706906.1:c.*2145+7T=	ENSP00000516618.1:n.*2145+7T=
ENST00000308192.14:c.2125+7T= MANE Select	ENSP00000308938.9:n.2125+7T=
ENST00000308192.13:c.2125+7T=	ENSP00000308938.9:n.2125+7T=
ENST00000461414.2:n.99+56T=
ENST00000467466.1:n.426+7T=
NM_000301.3:c.2125+7T= , LRG_571t1:c.2125+7T=	NP_000292.1:n.2125+7T=
NM_000301.4:c.2125+7T=	NP_000292.1:n.2125+7T=
NM_000301.5:c.2125+7T= MANE Select	NP_000292.1:n.2125+7T=