Canonical Allele Identifier: CA1825399609
Community Standard Title: NM_005672.5(PSCA):c.133+80G=

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142681514G= , CM000670.2:g.142681514G= GRCh38
NC_000008.10:g.143762932G= , CM000670.1:g.143762932G= GRCh37
NC_000008.9:g.143759934G= NCBI36
NG_011722.2:g.6058G=
NG_011722.3:g.16207G=

Transcript Alleles

HGVS Amino-acid Change
NM_005672.5:c.133+80G= (PSCA) MANE Select NP_005663.2:n.133+80G=
ENST00000301258.5:c.133+80G= (PSCA) MANE Select ENSP00000301258.4:n.133+80G=
NM_005672.4:c.133+80G= (PSCA) NP_005663.2:n.133+80G=
NR_033343.1:n.369+80G= (PSCA)
NR_033343.2:n.380+80G= (PSCA)
ENST00000301258.4:c.133+80G= (PSCA) ENSP00000301258.4:n.133+80G=
ENST00000505305.1:n.449G= (PSCA)
ENST00000510969.1:n.356+80G= (PSCA)
ENST00000513264.1:c.*48G= (PSCA) ENSP00000426508.1:n.*48G=
ENST00000585503.1:n.264+191C= (JRK)
ENST00000587499.1:n.100+191C= (JRK)
ENST00000587883.5:n.264+191C= (JRK)
ENST00000591180.5:n.130+191C= (JRK)
ENST00000591357.5:n.264+191C= (JRK)