Canonical Allele Identifier: CA1825399213

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142681306C>T , CM000670.2:g.142681306C>T GRCh38
NC_000008.10:g.143762724C>T , CM000670.1:g.143762724C>T GRCh37
NC_000008.9:g.143759726C>T NCBI36
NG_011722.2:g.5850C>T
NG_011722.3:g.15999C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301258.5:c.26-21C>T (PSCA) MANE Select ENSP00000301258.4:n.26-21C>T
ENST00000301258.4:c.26-21C>T (PSCA) ENSP00000301258.4:n.26-21C>T
ENST00000505305.1:n.262-21C>T (PSCA)
ENST00000510969.1:n.249-21C>T (PSCA)
ENST00000513264.1:c.26-21C>T (PSCA) ENSP00000426508.1:n.26-21C>T
ENST00000585503.1:n.264+399G>A (JRK)
ENST00000587499.1:n.101-169G>A (JRK)
ENST00000587883.5:n.264+399G>A (JRK)
ENST00000591180.5:n.130+399G>A (JRK)
ENST00000591357.5:n.264+399G>A (JRK)
NM_005672.4:c.26-21C>T (PSCA) NP_005663.2:n.26-21C>T
NR_033343.1:n.262-21C>T (PSCA)
NM_005672.5:c.26-21C>T (PSCA) MANE Select NP_005663.2:n.26-21C>T
NR_033343.2:n.273-21C>T (PSCA)