Canonical Allele Identifier: CA1748637025

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142774274_142774275delinsGC , CM000669.2:g.142774274_142774275delinsGC GRCh38
NC_000007.12:g.142182077_142182078delinsGC NCBI36
NG_008322.2:g.8332_8333delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000539842.6:c.592-82_592-81delinsGC (PRSS2) MANE Select ENSP00000488338.1:n.592-82_592-81delinsGC
ENST00000539842.5:c.592-82_592-81delinsGC (PRSS2) ENSP00000488338.1:n.592-82_592-81delinsGC
ENST00000610416.2:c.371-12764_371-12763delinsGC (TRBC1) ENSP00000482915.1:n.371-12764_371-12763delinsGC
ENST00000618750.2:n.425-82_425-81delinsGC (PRSS2)
ENST00000632805.1:c.589-82_589-81delinsGC (PRSS2) ENSP00000488077.1:n.589-82_589-81delinsGC
ENST00000632998.1:c.592-82_592-81delinsGC (PRSS2) ENSP00000488789.1:n.592-82_592-81delinsGC
ENST00000633114.1:c.598-82_598-81delinsGC (PRSS2) ENSP00000487822.1:n.598-82_598-81delinsGC
ENST00000633969.1:c.634-82_634-81delinsGC (PRSS2) ENSP00000488437.1:n.634-82_634-81delinsGC
ENST00000634019.1:c.634-82_634-81delinsGC (PRSS2) ENSP00000488594.1:n.634-82_634-81delinsGC
NM_001303414.1:c.634-82_634-81delinsGC (PRSS2) NP_001290343.1:n.634-82_634-81delinsGC
NM_002770.3:c.592-82_592-81delinsGC (PRSS2) NP_002761.1:n.592-82_592-81delinsGC
NR_130149.1:n.558-82_558-81delinsGC (PRSS2)
NM_002770.4:c.592-82_592-81delinsGC (PRSS2) MANE Select NP_002761.1:n.592-82_592-81delinsGC
NR_130149.2:n.531-82_531-81delinsGC (PRSS2)
NM_001303414.2:c.634-82_634-81delinsGC (PRSS2) NP_001290343.1:n.634-82_634-81delinsGC