Canonical Allele Identifier: CA744847638

Gene: PLTP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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