Canonical Allele Identifier: CA410440610
Community Standard Title: NM_144991.3(TSPEAR):c.1093C>T (p.Gln365Ter)
Gene: TSPEAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44527348G>A , CM000683.2:g.44527348G>A GRCh38
NC_000021.8:g.45947231G>A , CM000683.1:g.45947231G>A GRCh37
NC_000021.7:g.44771659G>A NCBI36
NG_033806.1:g.189231C>T

Transcript Alleles

HGVS Amino-acid Change
NM_144991.3:c.1093C>T MANE Select NP_659428.2:p.Gln365Ter
ENST00000323084.9:c.1093C>T MANE Select ENSP00000321987.4:p.Gln365Ter
NM_001272037.1:c.889C>T NP_001258966.1:p.Gln297Ter
NM_001272037.2:c.889C>T NP_001258966.1:p.Gln297Ter
NM_144991.2:c.1093C>T NP_659428.2:p.Gln365Ter
ENST00000323084.8:c.1093C>T ENSP00000321987.4:p.Gln365Ter
ENST00000397916.1:c.889C>T ENSP00000381012.1:p.Gln297Ter
ENST00000613245.4:c.652C>T ENSP00000478010.1:p.Gln218Ter
ENST00000614657.4:c.889C>T ENSP00000482422.1:p.Gln297Ter
ENST00000642437.1:c.*1038C>T ENSP00000496535.1:n.*1038C>T