Canonical Allele Identifier: CA2715876463

Linked Data

dbSNP Id: rs2116995460

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753944dup , CM000669.2:g.142753944dup GRCh38
NC_000007.13:g.142461795dup , CM000669.1:g.142461795dup GRCh37
NC_000007.12:g.142141369dup NCBI36
NG_008307.3:g.9461dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32758dup (TRBC1) ENSP00000482915.1:n.370+32758dup
ENST00000612126.4:c.591+1377dup (PRSS1) ENSP00000479959.1:n.591+1377dup
ENST00000633114.1:c.321+2050dup (PRSS2) ENSP00000487822.1:n.321+2050dup
ENST00000634019.1:c.82+5153dup (PRSS2) ENSP00000488594.1:n.82+5153dup