Canonical Allele Identifier: CA1748624052

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752309_142752311delinsTTA , CM000669.2:g.142752309_142752311delinsTTA GRCh38
NC_000007.13:g.142460160_142460162delinsTTA , CM000669.1:g.142460160_142460162delinsTTA GRCh37
NC_000007.12:g.142139734_142139736delinsTTA NCBI36
NG_008307.3:g.7826_7828delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.455-122_455-120delinsTTA (PRSS1) MANE Select ENSP00000308720.7:n.455-122_455-120delinsTTA
ENST00000311737.11:c.455-122_455-120delinsTTA (PRSS1) ENSP00000308720.7:n.455-122_455-120delinsTTA
ENST00000463701.1:n.919-122_919-120delinsTTA (PRSS1)
ENST00000486171.5:c.497-122_497-120delinsTTA (PRSS1) ENSP00000417854.1:n.497-122_497-120delinsTTA
ENST00000492062.1:c.305-122_305-120delinsTTA (PRSS1) ENSP00000419912.1:n.305-122_305-120delinsTTA
ENST00000610416.2:c.370+31123_370+31125delinsTTA (TRBC1) ENSP00000482915.1:n.370+31123_370+31125delinsTTA
ENST00000612126.4:c.455-122_455-120delinsTTA (PRSS1) ENSP00000479959.1:n.455-122_455-120delinsTTA
ENST00000619214.4:c.425-122_425-120delinsTTA (PRSS1) ENSP00000481361.1:n.425-122_425-120delinsTTA
ENST00000633114.1:c.321+415_321+417delinsTTA (PRSS2) ENSP00000487822.1:n.321+415_321+417delinsTTA
ENST00000634019.1:c.82+3518_82+3520delinsTTA (PRSS2) ENSP00000488594.1:n.82+3518_82+3520delinsTTA
NM_002769.4:c.455-122_455-120delinsTTA (PRSS1) NP_002760.1:n.455-122_455-120delinsTTA
XM_011516411.1:c.1130-122_1130-120delinsTTA (PRSS1) XP_011514713.1:n.1130-122_1130-120delinsTTA
NM_002769.5:c.455-122_455-120delinsTTA (PRSS1) MANE Select NP_002760.1:n.455-122_455-120delinsTTA
NR_172947.1:n.397-122_397-120delinsTTA (PRSS1)
NR_172948.1:n.394-122_394-120delinsTTA (PRSS1)
NR_172949.1:n.394-122_394-120delinsTTA (PRSS1)
NR_172950.1:n.308-122_308-120delinsTTA (PRSS1)
NR_172951.1:n.242-122_242-120delinsTTA (PRSS1)