Canonical Allele Identifier: CA410436972
Community Standard Title: NM_144991.3(TSPEAR):c.1463C>A (p.Ser488Ter)
Gene: TSPEAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44521986G>T , CM000683.2:g.44521986G>T GRCh38
NC_000021.8:g.45941869G>T , CM000683.1:g.45941869G>T GRCh37
NC_000021.7:g.44766297G>T NCBI36
NG_033806.1:g.194593C>A

Transcript Alleles

HGVS Amino-acid Change
NM_144991.3:c.1463C>A MANE Select NP_659428.2:p.Ser488Ter
ENST00000323084.9:c.1463C>A MANE Select ENSP00000321987.4:p.Ser488Ter
NM_001272037.1:c.1259C>A NP_001258966.1:p.Ser420Ter
NM_001272037.2:c.1259C>A NP_001258966.1:p.Ser420Ter
NM_144991.2:c.1463C>A NP_659428.2:p.Ser488Ter
ENST00000323084.8:c.1463C>A ENSP00000321987.4:p.Ser488Ter
ENST00000397916.1:c.1259C>A ENSP00000381012.1:p.Ser420Ter
ENST00000613245.4:c.1022C>A ENSP00000478010.1:p.Ser341Ter
ENST00000614657.4:c.1259C>A ENSP00000482422.1:p.Ser420Ter
ENST00000642437.1:c.*1408C>A ENSP00000496535.1:n.*1408C>A