Canonical Allele Identifier: CA6047680
Gene: TUT1 HGNC NCBI

Linked Data

dbSNP Id: rs772768932
ExAC: 11:62344369 G / A
gnomAD v2: 11-62344369-G-A
gnomAD v3: 11-62576897-G-A
gnomAD v4: 11-62576897-G-A
MyVariant Identifiers: chr11:g.62344369G>A (hg19) chr11:g.62576897G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62576897G>A , CM000673.2:g.62576897G>A GRCh38
NC_000011.9:g.62344369G>A , CM000673.1:g.62344369G>A GRCh37
NC_000011.8:g.62100945G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000476907.6:c.1381+10C>T MANE Select ENSP00000419607.1:n.1381+10C>T
ENST00000308436.11:c.1495+10C>T ENSP00000308000.7:n.1495+10C>T
ENST00000463241.2:n.246+10C>T
ENST00000469480.1:n.197C>T
ENST00000476907.5:c.1381+10C>T ENSP00000419607.1:n.1381+10C>T
ENST00000496634.2:c.1381+10C>T ENSP00000456163.1:n.1381+10C>T
ENST00000526409.5:n.251+10C>T
NM_022830.2:c.1495+10C>T NP_073741.2:n.1495+10C>T
NM_001367906.1:c.1322+10C>T NP_001354835.1:n.1322+10C>T
NM_022830.3:c.1381+10C>T MANE Select NP_073741.3:n.1381+10C>T
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