Canonical Allele Identifier: CA342998

Linked Data

dbSNP Id: rs397507441

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750577_142750585dup , CM000669.2:g.142750577_142750585dup GRCh38
NC_000007.13:g.142458428_142458436dup , CM000669.1:g.142458428_142458436dup GRCh37
NC_000007.12:g.142138002_142138010dup NCBI36
NG_008307.3:g.6094_6102dup

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.63_71dup (PRSS1) MANE Select ENSP00000308720.7:p.Ile24_Val25insAspLysI...
ENST00000311737.11:c.63_71dup (PRSS1) ENSP00000308720.7:p.Ile24_Val25insAspLysI...
ENST00000485223.1:n.54-52_54-44dup (PRSS1)
ENST00000486171.5:c.63_71dup (PRSS1) ENSP00000417854.1:p.Ile24_Val25insAspLysI...
ENST00000497041.1:n.67_75dup (PRSS1)
ENST00000610416.2:c.370+29391_370+29399dup (TRBC1) ENSP00000482915.1:n.370+29391_370+29399du...
ENST00000612126.4:c.63_71dup (PRSS1) ENSP00000479959.1:p.Ile24_Val25insAspLysI...
ENST00000619214.4:c.63_71dup (PRSS1) ENSP00000481361.1:p.Ile24_Val25insAspLysI...
ENST00000633114.1:c.63_71dup (PRSS2) ENSP00000487822.1:p.Ile24_Val25insAspLysI...
ENST00000634019.1:c.82+1786_82+1794dup (PRSS2) ENSP00000488594.1:n.82+1786_82+1794dup
NM_002769.4:c.63_71dup (PRSS1) NP_002760.1:p.Ile24_Val25insAspLysIle
XM_011516411.1:c.738_746dup (PRSS1) XP_011514713.1:p.Ile249_Val250insAspLysIl...
NM_002769.5:c.63_71dup (PRSS1) MANE Select NP_002760.1:p.Ile24_Val25insAspLysIle
NR_172947.1:n.76_84dup (PRSS1)
NR_172948.1:n.76_84dup (PRSS1)
NR_172949.1:n.54-52_54-44dup (PRSS1)
NR_172950.1:n.53+1053_53+1061dup (PRSS1)
NR_172951.1:n.54-52_54-44dup (PRSS1)