Canonical Allele Identifier: CA673395951

Gene: TOLLIP

Linked Data

• dbSNP Id: rs1345425036
• gnomAD v3: 11-1303495-C-T
• gnomAD v4: 11-1303495-C-T
• MyVariant Identifiers: chr11:g.1324725C>T (hg19) ; chr11:g.1303495C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1303495C>T , CM000673.2:g.1303495C>T	GRCh38
NC_000011.9:g.1324725C>T , CM000673.1:g.1324725C>T	GRCh37
NC_000011.8:g.1281301C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317204.11:c.33+5971G>A MANE Select	ENSP00000314733.5:n.33+5971G>A
ENST00000263646.11:c.12+5992G>A	ENSP00000263646.6:n.12+5992G>A
ENST00000317204.10:c.33+5971G>A	ENSP00000314733.5:n.33+5971G>A
ENST00000525159.5:c.33+5971G>A	ENSP00000432668.1:n.33+5971G>A
ENST00000527085.1:n.180-4931G>A
ENST00000527638.1:n.132+5971G>A
ENST00000527746.5:n.125+5971G>A
ENST00000527938.5:c.33+5971G>A	ENSP00000432778.1:n.33+5971G>A
ENST00000530506.5:c.33+5971G>A	ENSP00000436393.1:n.33+5971G>A
ENST00000530541.1:c.33+5971G>A	ENSP00000434494.1:n.33+5971G>A
ENST00000530821.1:n.372+2328G>A
ENST00000532551.1:n.158+5971G>A
NM_019009.3:c.33+5971G>A	NP_061882.2:n.33+5971G>A
NM_001318512.1:c.33+5971G>A	NP_001305441.1:n.33+5971G>A
NM_001318515.1:c.33+5971G>A	NP_001305444.1:n.33+5971G>A
NM_001318516.1:c.33+5971G>A	NP_001305445.1:n.33+5971G>A
XR_001747910.2:n.158+5971G>A
NM_019009.4:c.33+5971G>A MANE Select	NP_061882.2:n.33+5971G>A
NM_001318512.2:c.33+5971G>A	NP_001305441.1:n.33+5971G>A
NM_001318515.2:c.33+5971G>A	NP_001305444.1:n.33+5971G>A
NM_001318516.2:c.33+5971G>A	NP_001305445.1:n.33+5971G>A