Canonical Allele Identifier: CA369607531

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750695G>A , CM000669.2:g.142750695G>A GRCh38
NC_000007.13:g.142458546G>A , CM000669.1:g.142458546G>A GRCh37
NC_000007.12:g.142138120G>A NCBI36
NG_008307.3:g.6212G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.181G>A (PRSS1) MANE Select ENSP00000308720.7:p.Ala61Thr
ENST00000311737.11:c.181G>A (PRSS1) ENSP00000308720.7:p.Ala61Thr
ENST00000485223.1:n.120G>A (PRSS1)
ENST00000486171.5:c.181G>A (PRSS1) ENSP00000417854.1:p.Ala61Thr
ENST00000492062.1:c.31G>A (PRSS1) ENSP00000419912.1:p.Ala11Thr
ENST00000497041.1:n.185G>A (PRSS1)
ENST00000610416.2:c.370+29509G>A (TRBC1) ENSP00000482915.1:n.370+29509G>A
ENST00000612126.4:c.181G>A (PRSS1) ENSP00000479959.1:p.Ala61Thr
ENST00000619214.4:c.181G>A (PRSS1) ENSP00000481361.1:p.Ala61Thr
ENST00000633114.1:c.181G>A (PRSS2) ENSP00000487822.1:p.Ala61Thr
ENST00000634019.1:c.82+1904G>A (PRSS2) ENSP00000488594.1:n.82+1904G>A
NM_002769.4:c.181G>A (PRSS1) NP_002760.1:p.Ala61Thr
XM_011516411.1:c.856G>A (PRSS1) XP_011514713.1:p.Ala286Thr
NM_002769.5:c.181G>A (PRSS1) MANE Select NP_002760.1:p.Ala61Thr
NR_172947.1:n.194G>A (PRSS1)
NR_172948.1:n.194G>A (PRSS1)
NR_172949.1:n.120G>A (PRSS1)
NR_172950.1:n.54-1079G>A (PRSS1)
NR_172951.1:n.120G>A (PRSS1)