Canonical Allele Identifier: CA1118986241
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

gnomAD v3: 8-127080151-A-AAATACCTTCCCTCTGCTT
gnomAD v4: 8-127080151-A-AAATACCTTCCCTCTGCTT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080151_127080152insAATACCTTCCCTCTGCTT , CM000670.2:g.127080151_127080152insAATACCTTCCCTCTGCTT GRCh38
NC_000008.10:g.128092396_128092397insAATACCTTCCCTCTGCTT , CM000670.1:g.128092396_128092397insAATACCTTCCCTCTGCTT GRCh37
NC_000008.9:g.128161578_128161579insAATACCTTCCCTCTGCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109833.1:n.278_279insAATACCTTCCCTCTGCTT (PRNCR1)
NR_119373.1:n.102-1019_102-1018insAAGCAGAGGGAAGGTATT (PCAT2)
Search 100 bp 5'
Search 100 bp 3'