Canonical Allele Identifier: CA1169462466
Gene: TACSTD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576729A= , CM000663.2:g.58576729A= GRCh38
NC_000001.10:g.59042401A= , CM000663.1:g.59042401A= GRCh37
NC_000001.9:g.58814989A= NCBI36
NG_016237.1:g.5766T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.428T= MANE Select ENSP00000360269.2:p.Leu143=
ENST00000371225.3:c.428T= ENSP00000360269.2:p.Leu143=
NM_002353.2:c.428T= NP_002344.2:p.Leu143=
NM_002353.3:c.428T= MANE Select NP_002344.2:p.Leu143=
Search 100 bp 5'
Search 100 bp 3'