Canonical Allele Identifier: CA2685351961

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142774219_142774220insGCTTGGATTCAGCC , CM000669.2:g.142774219_142774220insGCTTGGATTCAGCC GRCh38
NC_000007.13:g.142482079_142482080insGCTTGGATTCAGCC , CM000669.1:g.142482079_142482080insGCTTGGATTCAGCC GRCh37
NC_000007.12:g.142182022_142182023insGCTTGGATTCAGCC NCBI36
NG_008322.2:g.8277_8278insGCTTGGATTCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000539842.6:c.592-137_592-136insGCTTGGATTCAGCC (PRSS2) MANE Select ENSP00000488338.1:n.592-137_592-136insGCTTGGATTCAGCC
ENST00000539842.5:c.592-137_592-136insGCTTGGATTCAGCC (PRSS2) ENSP00000488338.1:n.592-137_592-136insGCTTGGATTCAGCC
ENST00000610416.2:c.371-12819_371-12818insGCTTGGATTCAGCC (TRBC1) ENSP00000482915.1:n.371-12819_371-12818insGCTTGGATTCAGCC
ENST00000618750.2:n.425-137_425-136insGCTTGGATTCAGCC (PRSS2)
ENST00000632805.1:c.589-137_589-136insGCTTGGATTCAGCC (PRSS2) ENSP00000488077.1:n.589-137_589-136insGCTTGGATTCAGCC
ENST00000632998.1:c.592-137_592-136insGCTTGGATTCAGCC (PRSS2) ENSP00000488789.1:n.592-137_592-136insGCTTGGATTCAGCC
ENST00000633114.1:c.598-137_598-136insGCTTGGATTCAGCC (PRSS2) ENSP00000487822.1:n.598-137_598-136insGCTTGGATTCAGCC
ENST00000633969.1:c.634-137_634-136insGCTTGGATTCAGCC (PRSS2) ENSP00000488437.1:n.634-137_634-136insGCTTGGATTCAGCC
ENST00000634019.1:c.634-137_634-136insGCTTGGATTCAGCC (PRSS2) ENSP00000488594.1:n.634-137_634-136insGCTTGGATTCAGCC
NM_001303414.1:c.634-137_634-136insGCTTGGATTCAGCC (PRSS2) NP_001290343.1:n.634-137_634-136insGCTTGGATTCAGCC
NM_002770.3:c.592-137_592-136insGCTTGGATTCAGCC (PRSS2) NP_002761.1:n.592-137_592-136insGCTTGGATTCAGCC
NR_130149.1:n.558-137_558-136insGCTTGGATTCAGCC (PRSS2)
NM_002770.4:c.592-137_592-136insGCTTGGATTCAGCC (PRSS2) MANE Select NP_002761.1:n.592-137_592-136insGCTTGGATTCAGCC
NR_130149.2:n.531-137_531-136insGCTTGGATTCAGCC (PRSS2)
NM_001303414.2:c.634-137_634-136insGCTTGGATTCAGCC (PRSS2) NP_001290343.1:n.634-137_634-136insGCTTGGATTCAGCC