Canonical Allele Identifier: CA1108082733

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753940_142753941insTGCA , CM000669.2:g.142753940_142753941insTGCA GRCh38
NC_000007.13:g.142461791_142461792insTGCA , CM000669.1:g.142461791_142461792insTGCA GRCh37
NC_000007.12:g.142141365_142141366insTGCA NCBI36
NG_008307.3:g.9457_9458insTGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32754_370+32755insTGCA (TRBC1) ENSP00000482915.1:n.370+32754_370+32755insTGCA
ENST00000612126.4:c.591+1373_591+1374insTGCA (PRSS1) ENSP00000479959.1:n.591+1373_591+1374insTGCA
ENST00000633114.1:c.321+2046_321+2047insTGCA (PRSS2) ENSP00000487822.1:n.321+2046_321+2047insTGCA
ENST00000634019.1:c.82+5149_82+5150insTGCA (PRSS2) ENSP00000488594.1:n.82+5149_82+5150insTGCA