Canonical Allele Identifier: CA1825399613
Gene: PSCA HGNC NCBI
JRK HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000301258.5:c.133+80G>T (PSCA) MANE Select ENSP00000301258.4:n.133+80G>T
ENST00000301258.4:c.133+80G>T (PSCA) ENSP00000301258.4:n.133+80G>T
ENST00000505305.1:n.449G>T (PSCA)
ENST00000510969.1:n.356+80G>T (PSCA)
ENST00000513264.1:c.*48G>T (PSCA) ENSP00000426508.1:n.*48G>T
ENST00000585503.1:n.264+191C>A (JRK)
ENST00000587499.1:n.100+191C>A (JRK)
ENST00000587883.5:n.264+191C>A (JRK)
ENST00000591180.5:n.130+191C>A (JRK)
ENST00000591357.5:n.264+191C>A (JRK)
NM_005672.4:c.133+80G>T (PSCA) NP_005663.2:n.133+80G>T
NR_033343.1:n.369+80G>T (PSCA)
NM_005672.5:c.133+80G>T (PSCA) MANE Select NP_005663.2:n.133+80G>T
NR_033343.2:n.380+80G>T (PSCA)
Search 100 bp 5'
Search 100 bp 3'