Canonical Allele Identifier: CA1677212368

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160752240G= , CM000668.2:g.160752240G=	GRCh38
NC_000006.11:g.161173272G= , CM000668.1:g.161173272G=	GRCh37
NC_000006.10:g.161093262G=	NCBI36
NG_016200.1:g.55048G= , LRG_571:g.55048G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000301.5:c.2251G= MANE Select	NP_000292.1:p.Gly751=
ENST00000308192.14:c.2251G= MANE Select	ENSP00000308938.9:p.Gly751=
NM_000301.3:c.2251G= , LRG_571t1:c.2251G=	NP_000292.1:p.Gly751=
NM_000301.4:c.2251G=	NP_000292.1:p.Gly751=
ENST00000297289.9:c.1204G=	ENSP00000516619.1:p.Gly402=
ENST00000308192.13:c.2251G=	ENSP00000308938.9:p.Gly751=
ENST00000418964.2:c.2302G=	ENSP00000389424.2:p.Gly768=
ENST00000461414.2:n.225G=
ENST00000467466.1:n.552G=
ENST00000706906.1:c.*2271G=	ENSP00000516618.1:n.*2271G=