Canonical Allele Identifier: CA2366427132

Gene: PLTP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45906012G= , CM000682.2:g.45906012G=	GRCh38
NC_000020.10:g.44534651G= , CM000682.1:g.44534651G=	GRCh37
NC_000020.9:g.43968058G=	NCBI36
NG_012115.1:g.11136C=
NG_012115.2:g.11136C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006227.4:c.705+256C= MANE Select	NP_006218.1:n.705+256C=
ENST00000372431.8:c.705+256C= MANE Select	ENSP00000361508.3:n.705+256C=
NM_001242920.1:c.420+256C=	NP_001229849.1:n.420+256C=
NM_001242920.2:c.420+256C=	NP_001229849.1:n.420+256C=
NM_001242921.1:c.441+256C=	NP_001229850.1:n.441+256C=
NM_006227.3:c.705+256C=	NP_006218.1:n.705+256C=
NM_182676.2:c.549+256C=	NP_872617.1:n.549+256C=
NM_182676.3:c.549+256C=	NP_872617.1:n.549+256C=
ENST00000354050.8:c.549+256C=	ENSP00000335290.4:n.549+256C=
ENST00000372420.5:c.441+256C=	ENSP00000361497.1:n.441+256C=
ENST00000372431.7:c.705+256C=	ENSP00000361508.3:n.705+256C=
ENST00000420868.2:c.420+256C=	ENSP00000411671.2:n.420+256C=
ENST00000477313.5:c.705+256C=	ENSP00000417138.1:n.705+256C=