Canonical Allele Identifier: CA1825401778

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142680513C= , CM000670.2:g.142680513C= GRCh38
NC_000008.10:g.143761931C= , CM000670.1:g.143761931C= GRCh37
NC_000008.9:g.143758933C= NCBI36
NG_011722.2:g.5057C=
NG_011722.3:g.15206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301258.5:c.-26C= (PSCA) MANE Select ENSP00000301258.4:n.-26C=
ENST00000301258.4:c.-26C= (PSCA) ENSP00000301258.4:n.-26C=
ENST00000505305.1:n.262-814C= (PSCA)
ENST00000510969.1:n.249-814C= (PSCA)
ENST00000513264.1:c.-26C= (PSCA) ENSP00000426508.1:n.-26C=
ENST00000585503.1:n.636G= (JRK)
ENST00000587499.1:n.725G= (JRK)
ENST00000587883.5:n.264+1192G= (JRK)
ENST00000591180.5:n.130+1192G= (JRK)
ENST00000591357.5:n.264+1192G= (JRK)
NM_005672.4:c.-26C= (PSCA) NP_005663.2:n.-26C=
NR_033343.1:n.262-814C= (PSCA)
NM_005672.5:c.-26C= (PSCA) MANE Select NP_005663.2:n.-26C=
NR_033343.2:n.273-814C= (PSCA)