Canonical Allele Identifier: CA410437180
Community Standard Title: NM_144991.3(TSPEAR):c.1423G>C (p.Gly475Arg)
Gene: TSPEAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44522026C>G , CM000683.2:g.44522026C>G GRCh38
NC_000021.8:g.45941909C>G , CM000683.1:g.45941909C>G GRCh37
NC_000021.7:g.44766337C>G NCBI36
NG_033806.1:g.194553G>C

Transcript Alleles

HGVS Amino-acid Change
NM_144991.3:c.1423G>C MANE Select NP_659428.2:p.Gly475Arg
ENST00000323084.9:c.1423G>C MANE Select ENSP00000321987.4:p.Gly475Arg
NM_001272037.1:c.1219G>C NP_001258966.1:p.Gly407Arg
NM_001272037.2:c.1219G>C NP_001258966.1:p.Gly407Arg
NM_144991.2:c.1423G>C NP_659428.2:p.Gly475Arg
ENST00000323084.8:c.1423G>C ENSP00000321987.4:p.Gly475Arg
ENST00000397916.1:c.1219G>C ENSP00000381012.1:p.Gly407Arg
ENST00000613245.4:c.982G>C ENSP00000478010.1:p.Gly328Arg
ENST00000614657.4:c.1219G>C ENSP00000482422.1:p.Gly407Arg
ENST00000642437.1:c.*1368G>C ENSP00000496535.1:n.*1368G>C