Canonical Allele Identifier: CA1748622318

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142749847T= , CM000669.2:g.142749847T= GRCh38
NC_000007.13:g.142457698T= , CM000669.1:g.142457698T= GRCh37
NC_000007.12:g.142137272T= NCBI36
NG_008307.3:g.5364T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.40+323T= (PRSS1) MANE Select ENSP00000308720.7:n.40+323T=
ENST00000311737.11:c.40+323T= (PRSS1) ENSP00000308720.7:n.40+323T=
ENST00000485223.1:n.53+323T= (PRSS1)
ENST00000486171.5:c.40+323T= (PRSS1) ENSP00000417854.1:n.40+323T=
ENST00000497041.1:n.44+323T= (PRSS1)
ENST00000610416.2:c.370+28661T= (TRBC1) ENSP00000482915.1:n.370+28661T=
ENST00000612126.4:c.40+323T= (PRSS1) ENSP00000479959.1:n.40+323T=
ENST00000619214.4:c.40+323T= (PRSS1) ENSP00000481361.1:n.40+323T=
ENST00000633114.1:c.40+323T= (PRSS2) ENSP00000487822.1:n.40+323T=
ENST00000634019.1:c.82+1056T= (PRSS2) ENSP00000488594.1:n.82+1056T=
NM_002769.4:c.40+323T= (PRSS1) NP_002760.1:n.40+323T=
XM_011516411.1:c.715+323T= (PRSS1) XP_011514713.1:n.715+323T=
NM_002769.5:c.40+323T= (PRSS1) MANE Select NP_002760.1:n.40+323T=
NR_172947.1:n.53+323T= (PRSS1)
NR_172948.1:n.53+323T= (PRSS1)
NR_172949.1:n.53+323T= (PRSS1)
NR_172950.1:n.53+323T= (PRSS1)
NR_172951.1:n.53+323T= (PRSS1)