Canonical Allele Identifier: CA2778215843

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752082_142752083insCACCC , CM000669.2:g.142752082_142752083insCACCC GRCh38
NC_000007.13:g.142459933_142459934insCACCC , CM000669.1:g.142459933_142459934insCACCC GRCh37
NC_000007.12:g.142139507_142139508insCACCC NCBI36
NG_008307.3:g.7599_7600insCACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.454+55_454+56insCACCC (PRSS1) MANE Select ENSP00000308720.7:n.454+55_454+56insCACCC
ENST00000311737.11:c.454+55_454+56insCACCC (PRSS1) ENSP00000308720.7:n.454+55_454+56insCACCC
ENST00000463701.1:n.918+55_918+56insCACCC (PRSS1)
ENST00000486171.5:c.496+55_496+56insCACCC (PRSS1) ENSP00000417854.1:n.496+55_496+56insCACCC
ENST00000492062.1:c.304+55_304+56insCACCC (PRSS1) ENSP00000419912.1:n.304+55_304+56insCACCC
ENST00000610416.2:c.370+30896_370+30897insCACCC (TRBC1) ENSP00000482915.1:n.370+30896_370+30897insCACCC
ENST00000612126.4:c.454+55_454+56insCACCC (PRSS1) ENSP00000479959.1:n.454+55_454+56insCACCC
ENST00000619214.4:c.424+55_424+56insCACCC (PRSS1) ENSP00000481361.1:n.424+55_424+56insCACCC
ENST00000633114.1:c.321+188_321+189insCACCC (PRSS2) ENSP00000487822.1:n.321+188_321+189insCACCC
ENST00000634019.1:c.82+3291_82+3292insCACCC (PRSS2) ENSP00000488594.1:n.82+3291_82+3292insCACCC
NM_002769.4:c.454+55_454+56insCACCC (PRSS1) NP_002760.1:n.454+55_454+56insCACCC
XM_011516411.1:c.1129+55_1129+56insCACCC (PRSS1) XP_011514713.1:n.1129+55_1129+56insCACCC
NM_002769.5:c.454+55_454+56insCACCC (PRSS1) MANE Select NP_002760.1:n.454+55_454+56insCACCC
NR_172947.1:n.396+55_396+56insCACCC (PRSS1)
NR_172948.1:n.393+55_393+56insCACCC (PRSS1)
NR_172949.1:n.393+55_393+56insCACCC (PRSS1)
NR_172950.1:n.307+55_307+56insCACCC (PRSS1)
NR_172951.1:n.241+55_241+56insCACCC (PRSS1)