Canonical Allele Identifier: CA1677206037

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741433T= , CM000668.2:g.160741433T=	GRCh38
NC_000006.11:g.161162465T= , CM000668.1:g.161162465T=	GRCh37
NC_000006.10:g.161082455T=	NCBI36
NG_016200.1:g.44241T= , LRG_571:g.44241T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+16T=	ENSP00000516619.1:n.1078+16T=
ENST00000418964.2:c.2176+16T=	ENSP00000389424.2:n.2176+16T=
ENST00000706906.1:c.*2145+16T=	ENSP00000516618.1:n.*2145+16T=
ENST00000308192.14:c.2125+16T= MANE Select	ENSP00000308938.9:n.2125+16T=
ENST00000308192.13:c.2125+16T=	ENSP00000308938.9:n.2125+16T=
ENST00000461414.2:n.99+65T=
ENST00000467466.1:n.426+16T=
NM_000301.3:c.2125+16T= , LRG_571t1:c.2125+16T=	NP_000292.1:n.2125+16T=
NM_000301.4:c.2125+16T=	NP_000292.1:n.2125+16T=
NM_000301.5:c.2125+16T= MANE Select	NP_000292.1:n.2125+16T=