Canonical Allele Identifier: CA243471990

Gene: GLTP

Linked Data

• dbSNP Id: rs143073537
• gnomAD v3: 12-109874453-T-A
• gnomAD v4: 12-109874453-T-A
• MyVariant Identifiers: chr12:g.110312258T>A (hg19) ; chr12:g.109874453T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109874453T>A , CM000674.2:g.109874453T>A	GRCh38
NC_000012.11:g.110312258T>A , CM000674.1:g.110312258T>A	GRCh37
NC_000012.10:g.108796641T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318348.9:c.103+5819A>T MANE Select	ENSP00000315263.3:n.103+5819A>T
ENST00000537066.2:c.103+5819A>T	ENSP00000438128.1:n.103+5819A>T
ENST00000318348.8:c.103+5819A>T	ENSP00000315263.3:n.103+5819A>T
ENST00000536390.5:c.103+5819A>T	ENSP00000441537.1:n.103+5819A>T
ENST00000537066.1:c.103+5819A>T	ENSP00000438128.1:n.103+5819A>T
ENST00000540772.1:c.54+5819A>T
ENST00000544393.5:c.103+5819A>T	ENSP00000445919.1:n.103+5819A>T
ENST00000617457.4:c.103+5819A>T	ENSP00000481582.1:n.103+5819A>T
NM_016433.3:c.103+5819A>T	NP_057517.1:n.103+5819A>T
XM_011538434.1:c.-360+5819A>T	XP_011536736.1:n.-360+5819A>T
XM_011538434.3:c.-360+5819A>T	XP_011536736.1:n.-360+5819A>T
NM_016433.4:c.103+5819A>T MANE Select	NP_057517.1:n.103+5819A>T