Canonical Allele Identifier: CA1169462475
Gene: TACSTD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576744T= , CM000663.2:g.58576744T= GRCh38
NC_000001.10:g.59042416T= , CM000663.1:g.59042416T= GRCh37
NC_000001.9:g.58815004T= NCBI36
NG_016237.1:g.5751A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.413A= MANE Select ENSP00000360269.2:p.Lys138=
ENST00000371225.3:c.413A= ENSP00000360269.2:p.Lys138=
NM_002353.2:c.413A= NP_002344.2:p.Lys138=
NM_002353.3:c.413A= MANE Select NP_002344.2:p.Lys138=