Canonical Allele Identifier: CA380983634
Gene: TUT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62344464G>C (hg19) chr11:g.62576992G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62576992G>C , CM000673.2:g.62576992G>C GRCh38
NC_000011.9:g.62344464G>C , CM000673.1:g.62344464G>C GRCh37
NC_000011.8:g.62101040G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000476907.6:c.1296C>G MANE Select ENSP00000419607.1:p.Tyr432Ter
ENST00000308436.11:c.1410C>G ENSP00000308000.7:p.Tyr470Ter
ENST00000463241.2:n.161C>G
ENST00000469480.1:n.102C>G
ENST00000476907.5:c.1296C>G ENSP00000419607.1:p.Tyr432Ter
ENST00000496634.2:c.1296C>G ENSP00000456163.1:p.Tyr432Ter
ENST00000526409.5:n.166C>G
NM_022830.2:c.1410C>G NP_073741.2:p.Tyr470Ter
NM_001367906.1:c.1271-34C>G NP_001354835.1:n.1271-34C>G
NM_022830.3:c.1296C>G MANE Select NP_073741.3:p.Tyr432Ter
Search 100 bp 5'
Search 100 bp 3'