Canonical Allele Identifier: CA217031013

Gene: TOLLIP

Linked Data

• dbSNP Id: rs919162984
• gnomAD v2: 11-1325768-G-A
• gnomAD v3: 11-1304538-G-A
• gnomAD v4: 11-1304538-G-A
• MyVariant Identifiers: chr11:g.1325768G>A (hg19) ; chr11:g.1304538G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1304538G>A , CM000673.2:g.1304538G>A	GRCh38
NC_000011.9:g.1325768G>A , CM000673.1:g.1325768G>A	GRCh37
NC_000011.8:g.1282344G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317204.11:c.33+4928C>T MANE Select	ENSP00000314733.5:n.33+4928C>T
ENST00000263646.11:c.12+4949C>T	ENSP00000263646.6:n.12+4949C>T
ENST00000317204.10:c.33+4928C>T	ENSP00000314733.5:n.33+4928C>T
ENST00000525159.5:c.33+4928C>T	ENSP00000432668.1:n.33+4928C>T
ENST00000527085.1:n.179+4928C>T
ENST00000527638.1:n.132+4928C>T
ENST00000527746.5:n.125+4928C>T
ENST00000527938.5:c.33+4928C>T	ENSP00000432778.1:n.33+4928C>T
ENST00000530506.5:c.33+4928C>T	ENSP00000436393.1:n.33+4928C>T
ENST00000530541.1:c.33+4928C>T	ENSP00000434494.1:n.33+4928C>T
ENST00000530821.1:n.372+1285C>T
ENST00000532551.1:n.158+4928C>T
NM_019009.3:c.33+4928C>T	NP_061882.2:n.33+4928C>T
NM_001318512.1:c.33+4928C>T	NP_001305441.1:n.33+4928C>T
NM_001318515.1:c.33+4928C>T	NP_001305444.1:n.33+4928C>T
NM_001318516.1:c.33+4928C>T	NP_001305445.1:n.33+4928C>T
XR_001747910.2:n.158+4928C>T
NM_019009.4:c.33+4928C>T MANE Select	NP_061882.2:n.33+4928C>T
NM_001318512.2:c.33+4928C>T	NP_001305441.1:n.33+4928C>T
NM_001318515.2:c.33+4928C>T	NP_001305444.1:n.33+4928C>T
NM_001318516.2:c.33+4928C>T	NP_001305445.1:n.33+4928C>T