Canonical Allele Identifier: CA1169462502
Gene: TACSTD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576809C= , CM000663.2:g.58576809C= GRCh38
NC_000001.10:g.59042481C= , CM000663.1:g.59042481C= GRCh37
NC_000001.9:g.58815069C= NCBI36
NG_016237.1:g.5686G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.348G= MANE Select ENSP00000360269.2:p.Ala116=
ENST00000371225.3:c.348G= ENSP00000360269.2:p.Ala116=
NM_002353.2:c.348G= NP_002344.2:p.Ala116=
NM_002353.3:c.348G= MANE Select NP_002344.2:p.Ala116=
Search 100 bp 5'
Search 100 bp 3'