Canonical Allele Identifier: CA2366429995

Gene: PLTP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45912053C= , CM000682.2:g.45912053C=	GRCh38
NC_000020.10:g.44540692C= , CM000682.1:g.44540692C=	GRCh37
NC_000020.9:g.43974099C=	NCBI36
NG_012115.1:g.5095G=
NG_012115.2:g.5095G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006227.4:c.-12+26G= MANE Select	NP_006218.1:n.-12+26G=
ENST00000372431.8:c.-12+26G= MANE Select	ENSP00000361508.3:n.-12+26G=
NM_001242920.1:c.-12+26G=	NP_001229849.1:n.-12+26G=
NM_001242920.2:c.-12+26G=	NP_001229849.1:n.-12+26G=
NM_006227.3:c.-12+26G=	NP_006218.1:n.-12+26G=
NM_182676.2:c.-12+26G=	NP_872617.1:n.-12+26G=
NM_182676.3:c.-12+26G=	NP_872617.1:n.-12+26G=
ENST00000354050.8:c.-12+26G=	ENSP00000335290.4:n.-12+26G=
ENST00000372431.7:c.-12+26G=	ENSP00000361508.3:n.-12+26G=
ENST00000420868.2:c.-12+26G=	ENSP00000411671.2:n.-12+26G=