Canonical Allele Identifier: CA1677206040

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741441A= , CM000668.2:g.160741441A=	GRCh38
NC_000006.11:g.161162473A= , CM000668.1:g.161162473A=	GRCh37
NC_000006.10:g.161082463A=	NCBI36
NG_016200.1:g.44249A= , LRG_571:g.44249A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+24A=	ENSP00000516619.1:n.1078+24A=
ENST00000418964.2:c.2176+24A=	ENSP00000389424.2:n.2176+24A=
ENST00000706906.1:c.*2145+24A=	ENSP00000516618.1:n.*2145+24A=
ENST00000308192.14:c.2125+24A= MANE Select	ENSP00000308938.9:n.2125+24A=
ENST00000308192.13:c.2125+24A=	ENSP00000308938.9:n.2125+24A=
ENST00000461414.2:n.99+73A=
ENST00000467466.1:n.426+24A=
NM_000301.3:c.2125+24A= , LRG_571t1:c.2125+24A=	NP_000292.1:n.2125+24A=
NM_000301.4:c.2125+24A=	NP_000292.1:n.2125+24A=
NM_000301.5:c.2125+24A= MANE Select	NP_000292.1:n.2125+24A=