Canonical Allele Identifier: CA369609238

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752018A>C , CM000669.2:g.142752018A>C GRCh38
NC_000007.13:g.142459869A>C , CM000669.1:g.142459869A>C GRCh37
NC_000007.12:g.142139443A>C NCBI36
NG_008307.3:g.7535A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.445A>C (PRSS1) MANE Select ENSP00000308720.7:p.Ser149Arg
ENST00000311737.11:c.445A>C (PRSS1) ENSP00000308720.7:p.Ser149Arg
ENST00000463701.1:n.909A>C (PRSS1)
ENST00000486171.5:c.487A>C (PRSS1) ENSP00000417854.1:p.Ser163Arg
ENST00000492062.1:c.295A>C (PRSS1) ENSP00000419912.1:p.Ser99Arg
ENST00000610416.2:c.370+30832A>C (TRBC1) ENSP00000482915.1:n.370+30832A>C
ENST00000612126.4:c.445A>C (PRSS1) ENSP00000479959.1:p.Ser149Arg
ENST00000619214.4:c.415A>C (PRSS1) ENSP00000481361.1:p.Ser139Arg
ENST00000633114.1:c.321+124A>C (PRSS2) ENSP00000487822.1:n.321+124A>C
ENST00000634019.1:c.82+3227A>C (PRSS2) ENSP00000488594.1:n.82+3227A>C
NM_002769.4:c.445A>C (PRSS1) NP_002760.1:p.Ser149Arg
XM_011516411.1:c.1120A>C (PRSS1) XP_011514713.1:p.Ser374Arg
NM_002769.5:c.445A>C (PRSS1) MANE Select NP_002760.1:p.Ser149Arg
NR_172947.1:n.387A>C (PRSS1)
NR_172948.1:n.384A>C (PRSS1)
NR_172949.1:n.384A>C (PRSS1)
NR_172950.1:n.298A>C (PRSS1)
NR_172951.1:n.232A>C (PRSS1)