Canonical Allele Identifier: CA2685349310

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752078_142752080del , CM000669.2:g.142752078_142752080del GRCh38
NC_000007.13:g.142459929_142459931del , CM000669.1:g.142459929_142459931del GRCh37
NC_000007.12:g.142139503_142139505del NCBI36
NG_008307.3:g.7595_7597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.454+51_454+53del (PRSS1) MANE Select ENSP00000308720.7:n.454+51_454+53del
ENST00000311737.11:c.454+51_454+53del (PRSS1) ENSP00000308720.7:n.454+51_454+53del
ENST00000463701.1:n.918+51_918+53del (PRSS1)
ENST00000486171.5:c.496+51_496+53del (PRSS1) ENSP00000417854.1:n.496+51_496+53del
ENST00000492062.1:c.304+51_304+53del (PRSS1) ENSP00000419912.1:n.304+51_304+53del
ENST00000610416.2:c.370+30892_370+30894del (TRBC1) ENSP00000482915.1:n.370+30892_370+30894del
ENST00000612126.4:c.454+51_454+53del (PRSS1) ENSP00000479959.1:n.454+51_454+53del
ENST00000619214.4:c.424+51_424+53del (PRSS1) ENSP00000481361.1:n.424+51_424+53del
ENST00000633114.1:c.321+184_321+186del (PRSS2) ENSP00000487822.1:n.321+184_321+186del
ENST00000634019.1:c.82+3287_82+3289del (PRSS2) ENSP00000488594.1:n.82+3287_82+3289del
NM_002769.4:c.454+51_454+53del (PRSS1) NP_002760.1:n.454+51_454+53del
XM_011516411.1:c.1129+51_1129+53del (PRSS1) XP_011514713.1:n.1129+51_1129+53del
NM_002769.5:c.454+51_454+53del (PRSS1) MANE Select NP_002760.1:n.454+51_454+53del
NR_172947.1:n.396+51_396+53del (PRSS1)
NR_172948.1:n.393+51_393+53del (PRSS1)
NR_172949.1:n.393+51_393+53del (PRSS1)
NR_172950.1:n.307+51_307+53del (PRSS1)
NR_172951.1:n.241+51_241+53del (PRSS1)