Canonical Allele Identifier: CA1748622863

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750581A= , CM000669.2:g.142750581A= GRCh38
NC_000007.13:g.142458432A= , CM000669.1:g.142458432A= GRCh37
NC_000007.12:g.142138006A= NCBI36
NG_008307.3:g.6098A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.67A= (PRSS1) MANE Select ENSP00000308720.7:p.Lys23=
ENST00000311737.11:c.67A= (PRSS1) ENSP00000308720.7:p.Lys23=
ENST00000485223.1:n.54-48A= (PRSS1)
ENST00000486171.5:c.67A= (PRSS1) ENSP00000417854.1:p.Lys23=
ENST00000497041.1:n.71A= (PRSS1)
ENST00000610416.2:c.370+29395A= (TRBC1) ENSP00000482915.1:n.370+29395A=
ENST00000612126.4:c.67A= (PRSS1) ENSP00000479959.1:p.Lys23=
ENST00000619214.4:c.67A= (PRSS1) ENSP00000481361.1:p.Lys23=
ENST00000633114.1:c.67A= (PRSS2) ENSP00000487822.1:p.Lys23=
ENST00000634019.1:c.82+1790A= (PRSS2) ENSP00000488594.1:n.82+1790A=
NM_002769.4:c.67A= (PRSS1) NP_002760.1:p.Lys23=
XM_011516411.1:c.742A= (PRSS1) XP_011514713.1:p.Lys248=
NM_002769.5:c.67A= (PRSS1) MANE Select NP_002760.1:p.Lys23=
NR_172947.1:n.80A= (PRSS1)
NR_172948.1:n.80A= (PRSS1)
NR_172949.1:n.54-48A= (PRSS1)
NR_172950.1:n.53+1057A= (PRSS1)
NR_172951.1:n.54-48A= (PRSS1)