Canonical Allele Identifier: CA1169462468
Gene: TACSTD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576736G= , CM000663.2:g.58576736G= GRCh38
NC_000001.10:g.59042408G= , CM000663.1:g.59042408G= GRCh37
NC_000001.9:g.58814996G= NCBI36
NG_016237.1:g.5759C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.421C= MANE Select ENSP00000360269.2:p.Leu141=
ENST00000371225.3:c.421C= ENSP00000360269.2:p.Leu141=
NM_002353.2:c.421C= NP_002344.2:p.Leu141=
NM_002353.3:c.421C= MANE Select NP_002344.2:p.Leu141=
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