Canonical Allele Identifier: CA380983301
Gene: TUT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62344378C>G (hg19) chr11:g.62576906C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62576906C>G , CM000673.2:g.62576906C>G GRCh38
NC_000011.9:g.62344378C>G , CM000673.1:g.62344378C>G GRCh37
NC_000011.8:g.62100954C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000476907.6:c.1381+1G>C MANE Select ENSP00000419607.1:n.1381+1G>C
ENST00000308436.11:c.1495+1G>C ENSP00000308000.7:n.1495+1G>C
ENST00000463241.2:n.246+1G>C
ENST00000469480.1:n.188G>C
ENST00000476907.5:c.1381+1G>C ENSP00000419607.1:n.1381+1G>C
ENST00000496634.2:c.1381+1G>C ENSP00000456163.1:n.1381+1G>C
ENST00000526409.5:n.251+1G>C
NM_022830.2:c.1495+1G>C NP_073741.2:n.1495+1G>C
NM_001367906.1:c.1322+1G>C NP_001354835.1:n.1322+1G>C
NM_022830.3:c.1381+1G>C MANE Select NP_073741.3:n.1381+1G>C
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