Canonical Allele Identifier: CA1748623651

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751985A= , CM000669.2:g.142751985A= GRCh38
NC_000007.13:g.142459836A= , CM000669.1:g.142459836A= GRCh37
NC_000007.12:g.142139410A= NCBI36
NG_008307.3:g.7502A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311737.12:c.412A= (PRSS1) MANE Select ENSP00000308720.7:p.Lys138=
ENST00000311737.11:c.412A= (PRSS1) ENSP00000308720.7:p.Lys138=
ENST00000463701.1:n.876A= (PRSS1)
ENST00000485223.1:n.1410A= (PRSS1)
ENST00000486171.5:c.454A= (PRSS1) ENSP00000417854.1:p.Lys152=
ENST00000492062.1:c.262A= (PRSS1) ENSP00000419912.1:p.Lys88=
ENST00000610416.2:c.370+30799A= (TRBC1) ENSP00000482915.1:n.370+30799A=
ENST00000612126.4:c.412A= (PRSS1) ENSP00000479959.1:p.Lys138=
ENST00000619214.4:c.382A= (PRSS1) ENSP00000481361.1:p.Lys128=
ENST00000633114.1:c.321+91A= (PRSS2) ENSP00000487822.1:n.321+91A=
ENST00000634019.1:c.82+3194A= (PRSS2) ENSP00000488594.1:n.82+3194A=
NM_002769.4:c.412A= (PRSS1) NP_002760.1:p.Lys138=
XM_011516411.1:c.1087A= (PRSS1) XP_011514713.1:p.Lys363=
NM_002769.5:c.412A= (PRSS1) MANE Select NP_002760.1:p.Lys138=
NR_172947.1:n.354A= (PRSS1)
NR_172948.1:n.351A= (PRSS1)
NR_172949.1:n.351A= (PRSS1)
NR_172950.1:n.265A= (PRSS1)
NR_172951.1:n.199A= (PRSS1)