Canonical Allele Identifier: CA1748624045

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752290_142752292delinsCAG , CM000669.2:g.142752290_142752292delinsCAG GRCh38
NC_000007.13:g.142460141_142460143delinsCAG , CM000669.1:g.142460141_142460143delinsCAG GRCh37
NC_000007.12:g.142139715_142139717delinsCAG NCBI36
NG_008307.3:g.7807_7809delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.455-141_455-139delinsCAG (PRSS1) MANE Select ENSP00000308720.7:n.455-141_455-139delinsCAG
ENST00000311737.11:c.455-141_455-139delinsCAG (PRSS1) ENSP00000308720.7:n.455-141_455-139delinsCAG
ENST00000463701.1:n.919-141_919-139delinsCAG (PRSS1)
ENST00000486171.5:c.497-141_497-139delinsCAG (PRSS1) ENSP00000417854.1:n.497-141_497-139delinsCAG
ENST00000492062.1:c.305-141_305-139delinsCAG (PRSS1) ENSP00000419912.1:n.305-141_305-139delinsCAG
ENST00000610416.2:c.370+31104_370+31106delinsCAG (TRBC1) ENSP00000482915.1:n.370+31104_370+31106delinsCAG
ENST00000612126.4:c.455-141_455-139delinsCAG (PRSS1) ENSP00000479959.1:n.455-141_455-139delinsCAG
ENST00000619214.4:c.425-141_425-139delinsCAG (PRSS1) ENSP00000481361.1:n.425-141_425-139delinsCAG
ENST00000633114.1:c.321+396_321+398delinsCAG (PRSS2) ENSP00000487822.1:n.321+396_321+398delinsCAG
ENST00000634019.1:c.82+3499_82+3501delinsCAG (PRSS2) ENSP00000488594.1:n.82+3499_82+3501delinsCAG
NM_002769.4:c.455-141_455-139delinsCAG (PRSS1) NP_002760.1:n.455-141_455-139delinsCAG
XM_011516411.1:c.1130-141_1130-139delinsCAG (PRSS1) XP_011514713.1:n.1130-141_1130-139delinsCAG
NM_002769.5:c.455-141_455-139delinsCAG (PRSS1) MANE Select NP_002760.1:n.455-141_455-139delinsCAG
NR_172947.1:n.397-141_397-139delinsCAG (PRSS1)
NR_172948.1:n.394-141_394-139delinsCAG (PRSS1)
NR_172949.1:n.394-141_394-139delinsCAG (PRSS1)
NR_172950.1:n.308-141_308-139delinsCAG (PRSS1)
NR_172951.1:n.242-141_242-139delinsCAG (PRSS1)