Canonical Allele Identifier: CA1108082385

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753664_142753665insTGTTG , CM000669.2:g.142753664_142753665insTGTTG GRCh38
NC_000007.13:g.142461515_142461516insTGTTG , CM000669.1:g.142461515_142461516insTGTTG GRCh37
NC_000007.12:g.142141089_142141090insTGTTG NCBI36
NG_008307.3:g.9181_9182insTGTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32478_370+32479insTGTTG (TRBC1) ENSP00000482915.1:n.370+32478_370+32479insTGTTG
ENST00000612126.4:c.591+1097_591+1098insTGTTG (PRSS1) ENSP00000479959.1:n.591+1097_591+1098insTGTTG
ENST00000633114.1:c.321+1770_321+1771insTGTTG (PRSS2) ENSP00000487822.1:n.321+1770_321+1771insTGTTG
ENST00000634019.1:c.82+4873_82+4874insTGTTG (PRSS2) ENSP00000488594.1:n.82+4873_82+4874insTGTTG