Canonical Allele Identifier: CA1748623626

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751976A= , CM000669.2:g.142751976A= GRCh38
NC_000007.13:g.142459827A= , CM000669.1:g.142459827A= GRCh37
NC_000007.12:g.142139401A= NCBI36
NG_008307.3:g.7493A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.403A= (PRSS1) MANE Select ENSP00000308720.7:p.Thr135=
ENST00000311737.11:c.403A= (PRSS1) ENSP00000308720.7:p.Thr135=
ENST00000463701.1:n.867A= (PRSS1)
ENST00000485223.1:n.1401A= (PRSS1)
ENST00000486171.5:c.445A= (PRSS1) ENSP00000417854.1:p.Thr149=
ENST00000492062.1:c.253A= (PRSS1) ENSP00000419912.1:p.Thr85=
ENST00000610416.2:c.370+30790A= (TRBC1) ENSP00000482915.1:n.370+30790A=
ENST00000612126.4:c.403A= (PRSS1) ENSP00000479959.1:p.Thr135=
ENST00000619214.4:c.373A= (PRSS1) ENSP00000481361.1:p.Thr125=
ENST00000633114.1:c.321+82A= (PRSS2) ENSP00000487822.1:n.321+82A=
ENST00000634019.1:c.82+3185A= (PRSS2) ENSP00000488594.1:n.82+3185A=
NM_002769.4:c.403A= (PRSS1) NP_002760.1:p.Thr135=
XM_011516411.1:c.1078A= (PRSS1) XP_011514713.1:p.Thr360=
NM_002769.5:c.403A= (PRSS1) MANE Select NP_002760.1:p.Thr135=
NR_172947.1:n.345A= (PRSS1)
NR_172948.1:n.342A= (PRSS1)
NR_172949.1:n.342A= (PRSS1)
NR_172950.1:n.256A= (PRSS1)
NR_172951.1:n.190A= (PRSS1)