Canonical Allele Identifier: CA2723274177
Gene: TOLLIP HGNC NCBI

Linked Data

dbSNP Id: rs2133930077

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1302371_1302387dup , CM000673.2:g.1302371_1302387dup GRCh38
NC_000011.9:g.1323601_1323617dup , CM000673.1:g.1323601_1323617dup GRCh37
NC_000011.8:g.1280177_1280193dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317204.11:c.34-6593_34-6577dup MANE Select ENSP00000314733.5:n.34-6593_34-6577dup
ENST00000263646.11:c.13-6656_13-6640dup ENSP00000263646.6:n.13-6656_13-6640dup
ENST00000317204.10:c.34-6593_34-6577dup ENSP00000314733.5:n.34-6593_34-6577dup
ENST00000525159.5:c.34-6593_34-6577dup ENSP00000432668.1:n.34-6593_34-6577dup
ENST00000527085.1:n.180-3823_180-3807dup
ENST00000527638.1:n.133-6593_133-6577dup
ENST00000527746.5:n.126-6593_126-6577dup
ENST00000527886.5:c.-175+197_-175+213dup ENSP00000434035.1:n.-175+197_-175+213dup
ENST00000527938.5:c.34-6593_34-6577dup ENSP00000432778.1:n.34-6593_34-6577dup
ENST00000530506.5:c.33+7079_33+7095dup ENSP00000436393.1:n.33+7079_33+7095dup
ENST00000530541.1:c.33+7079_33+7095dup ENSP00000434494.1:n.33+7079_33+7095dup
ENST00000530821.1:n.372+3436_372+3452dup
ENST00000532551.1:n.159-6593_159-6577dup
NM_019009.3:c.34-6593_34-6577dup NP_061882.2:n.34-6593_34-6577dup
XM_011520192.1:c.-175+197_-175+213dup XP_011518494.1:n.-175+197_-175+213dup
XR_930968.1:n.188_204dup
NM_001318512.1:c.33+7079_33+7095dup NP_001305441.1:n.33+7079_33+7095dup
NM_001318514.1:c.-175+197_-175+213dup NP_001305443.1:n.-175+197_-175+213dup
NM_001318515.1:c.34-6593_34-6577dup NP_001305444.1:n.34-6593_34-6577dup
NM_001318516.1:c.34-6593_34-6577dup NP_001305445.1:n.34-6593_34-6577dup
XR_001747910.2:n.159-6593_159-6577dup
XR_930968.2:n.190_206dup
NM_019009.4:c.34-6593_34-6577dup MANE Select NP_061882.2:n.34-6593_34-6577dup
NM_001318512.2:c.33+7079_33+7095dup NP_001305441.1:n.33+7079_33+7095dup
NM_001318515.2:c.34-6593_34-6577dup NP_001305444.1:n.34-6593_34-6577dup
NM_001318516.2:c.34-6593_34-6577dup NP_001305445.1:n.34-6593_34-6577dup
NM_001318514.2:c.-175+197_-175+213dup NP_001305443.1:n.-175+197_-175+213dup