Canonical Allele Identifier: CA217030433

Gene: TOLLIP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1303542T>A , CM000673.2:g.1303542T>A	GRCh38
NC_000011.9:g.1324772T>A , CM000673.1:g.1324772T>A	GRCh37
NC_000011.8:g.1281348T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317204.11:c.33+5924A>T MANE Select	ENSP00000314733.5:n.33+5924A>T
ENST00000263646.11:c.12+5945A>T	ENSP00000263646.6:n.12+5945A>T
ENST00000317204.10:c.33+5924A>T	ENSP00000314733.5:n.33+5924A>T
ENST00000525159.5:c.33+5924A>T	ENSP00000432668.1:n.33+5924A>T
ENST00000527085.1:n.180-4978A>T
ENST00000527638.1:n.132+5924A>T
ENST00000527746.5:n.125+5924A>T
ENST00000527938.5:c.33+5924A>T	ENSP00000432778.1:n.33+5924A>T
ENST00000530506.5:c.33+5924A>T	ENSP00000436393.1:n.33+5924A>T
ENST00000530541.1:c.33+5924A>T	ENSP00000434494.1:n.33+5924A>T
ENST00000530821.1:n.372+2281A>T
ENST00000532551.1:n.158+5924A>T
NM_019009.3:c.33+5924A>T	NP_061882.2:n.33+5924A>T
NM_001318512.1:c.33+5924A>T	NP_001305441.1:n.33+5924A>T
NM_001318515.1:c.33+5924A>T	NP_001305444.1:n.33+5924A>T
NM_001318516.1:c.33+5924A>T	NP_001305445.1:n.33+5924A>T
XR_001747910.2:n.158+5924A>T
NM_019009.4:c.33+5924A>T MANE Select	NP_061882.2:n.33+5924A>T
NM_001318512.2:c.33+5924A>T	NP_001305441.1:n.33+5924A>T
NM_001318515.2:c.33+5924A>T	NP_001305444.1:n.33+5924A>T
NM_001318516.2:c.33+5924A>T	NP_001305445.1:n.33+5924A>T