Canonical Allele Identifier: CA1748624368

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751895_142751896delinsAT , CM000669.2:g.142751895_142751896delinsAT GRCh38
NC_000007.13:g.142459746_142459747delinsAT , CM000669.1:g.142459746_142459747delinsAT GRCh37
NC_000007.12:g.142139320_142139321delinsAT NCBI36
NG_008307.3:g.7412_7413delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.322_323delinsAT (PRSS1) MANE Select ENSP00000308720.7:p.Ile108=
ENST00000311737.11:c.322_323delinsAT (PRSS1) ENSP00000308720.7:p.Ile108=
ENST00000463701.1:n.786_787delinsAT (PRSS1)
ENST00000485223.1:n.1320_1321delinsAT (PRSS1)
ENST00000486171.5:c.364_365delinsAT (PRSS1) ENSP00000417854.1:p.Ile122=
ENST00000492062.1:c.172_173delinsAT (PRSS1) ENSP00000419912.1:p.Ile58=
ENST00000610416.2:c.370+30709_370+30710delinsAT (TRBC1) ENSP00000482915.1:n.370+30709_370+30710delinsAT
ENST00000612126.4:c.322_323delinsAT (PRSS1) ENSP00000479959.1:p.Ile108=
ENST00000619214.4:c.292_293delinsAT (PRSS1) ENSP00000481361.1:p.Ile98=
ENST00000633114.1:c.321+1_321+2delinsAT (PRSS2) ENSP00000487822.1:n.321+1_321+2delinsAT
ENST00000634019.1:c.82+3104_82+3105delinsAT (PRSS2) ENSP00000488594.1:n.82+3104_82+3105delinsAT
NM_002769.4:c.322_323delinsAT (PRSS1) NP_002760.1:p.Ile108=
XM_011516411.1:c.997_998delinsAT (PRSS1) XP_011514713.1:p.Ile333=
NM_002769.5:c.322_323delinsAT (PRSS1) MANE Select NP_002760.1:p.Ile108=
NR_172947.1:n.264_265delinsAT (PRSS1)
NR_172948.1:n.261_262delinsAT (PRSS1)
NR_172949.1:n.261_262delinsAT (PRSS1)
NR_172950.1:n.175_176delinsAT (PRSS1)
NR_172951.1:n.140-31_140-30delinsAT (PRSS1)