Canonical Allele Identifier: CA1108082699

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753921_142753922insCA , CM000669.2:g.142753921_142753922insCA GRCh38
NC_000007.13:g.142461772_142461773insCA , CM000669.1:g.142461772_142461773insCA GRCh37
NC_000007.12:g.142141346_142141347insCA NCBI36
NG_008307.3:g.9438_9439insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32735_370+32736insCA (TRBC1) ENSP00000482915.1:n.370+32735_370+32736insCA
ENST00000612126.4:c.591+1354_591+1355insCA (PRSS1) ENSP00000479959.1:n.591+1354_591+1355insCA
ENST00000633114.1:c.321+2027_321+2028insCA (PRSS2) ENSP00000487822.1:n.321+2027_321+2028insCA
ENST00000634019.1:c.82+5130_82+5131insCA (PRSS2) ENSP00000488594.1:n.82+5130_82+5131insCA