Canonical Allele Identifier: CA1748623852

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752089_142752090delinsGC , CM000669.2:g.142752089_142752090delinsGC GRCh38
NC_000007.13:g.142459940_142459941delinsGC , CM000669.1:g.142459940_142459941delinsGC GRCh37
NC_000007.12:g.142139514_142139515delinsGC NCBI36
NG_008307.3:g.7606_7607delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.454+62_454+63delinsGC (PRSS1) MANE Select ENSP00000308720.7:n.454+62_454+63delinsGC
ENST00000311737.11:c.454+62_454+63delinsGC (PRSS1) ENSP00000308720.7:n.454+62_454+63delinsGC
ENST00000463701.1:n.918+62_918+63delinsGC (PRSS1)
ENST00000486171.5:c.496+62_496+63delinsGC (PRSS1) ENSP00000417854.1:n.496+62_496+63delinsGC
ENST00000492062.1:c.304+62_304+63delinsGC (PRSS1) ENSP00000419912.1:n.304+62_304+63delinsGC
ENST00000610416.2:c.370+30903_370+30904delinsGC (TRBC1) ENSP00000482915.1:n.370+30903_370+30904delinsGC
ENST00000612126.4:c.454+62_454+63delinsGC (PRSS1) ENSP00000479959.1:n.454+62_454+63delinsGC
ENST00000619214.4:c.424+62_424+63delinsGC (PRSS1) ENSP00000481361.1:n.424+62_424+63delinsGC
ENST00000633114.1:c.321+195_321+196delinsGC (PRSS2) ENSP00000487822.1:n.321+195_321+196delinsGC
ENST00000634019.1:c.82+3298_82+3299delinsGC (PRSS2) ENSP00000488594.1:n.82+3298_82+3299delinsGC
NM_002769.4:c.454+62_454+63delinsGC (PRSS1) NP_002760.1:n.454+62_454+63delinsGC
XM_011516411.1:c.1129+62_1129+63delinsGC (PRSS1) XP_011514713.1:n.1129+62_1129+63delinsGC
NM_002769.5:c.454+62_454+63delinsGC (PRSS1) MANE Select NP_002760.1:n.454+62_454+63delinsGC
NR_172947.1:n.396+62_396+63delinsGC (PRSS1)
NR_172948.1:n.393+62_393+63delinsGC (PRSS1)
NR_172949.1:n.393+62_393+63delinsGC (PRSS1)
NR_172950.1:n.307+62_307+63delinsGC (PRSS1)
NR_172951.1:n.241+62_241+63delinsGC (PRSS1)