Canonical Allele Identifier: CA1748623856

Linked Data

dbSNP Id: rs1798788734

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752093del , CM000669.2:g.142752093del GRCh38
NC_000007.13:g.142459944del , CM000669.1:g.142459944del GRCh37
NC_000007.12:g.142139518del NCBI36
NG_008307.3:g.7610del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.454+66del (PRSS1) MANE Select ENSP00000308720.7:n.454+66del
ENST00000311737.11:c.454+66del (PRSS1) ENSP00000308720.7:n.454+66del
ENST00000463701.1:n.918+66del (PRSS1)
ENST00000486171.5:c.496+66del (PRSS1) ENSP00000417854.1:n.496+66del
ENST00000492062.1:c.304+66del (PRSS1) ENSP00000419912.1:n.304+66del
ENST00000610416.2:c.370+30907del (TRBC1) ENSP00000482915.1:n.370+30907del
ENST00000612126.4:c.454+66del (PRSS1) ENSP00000479959.1:n.454+66del
ENST00000619214.4:c.424+66del (PRSS1) ENSP00000481361.1:n.424+66del
ENST00000633114.1:c.321+199del (PRSS2) ENSP00000487822.1:n.321+199del
ENST00000634019.1:c.82+3302del (PRSS2) ENSP00000488594.1:n.82+3302del
NM_002769.4:c.454+66del (PRSS1) NP_002760.1:n.454+66del
XM_011516411.1:c.1129+66del (PRSS1) XP_011514713.1:n.1129+66del
NM_002769.5:c.454+66del (PRSS1) MANE Select NP_002760.1:n.454+66del
NR_172947.1:n.396+66del (PRSS1)
NR_172948.1:n.393+66del (PRSS1)
NR_172949.1:n.393+66del (PRSS1)
NR_172950.1:n.307+66del (PRSS1)
NR_172951.1:n.241+66del (PRSS1)