Canonical Allele Identifier: CA1108082276

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753657_142753658insTTTTTTTTTT , CM000669.2:g.142753657_142753658insTTTTTTTTTT GRCh38
NC_000007.13:g.142461508_142461509insTTTTTTTTTT , CM000669.1:g.142461508_142461509insTTTTTTTTTT GRCh37
NC_000007.12:g.142141082_142141083insTTTTTTTTTT NCBI36
NG_008307.3:g.9174_9175insTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000610416.2:c.370+32471_370+32472insTTTTTTTTTT (TRBC1) ENSP00000482915.1:n.370+32471_370+32472insTTTTTTTTTT
ENST00000612126.4:c.591+1090_591+1091insTTTTTTTTTT (PRSS1) ENSP00000479959.1:n.591+1090_591+1091insTTTTTTTTTT
ENST00000633114.1:c.321+1763_321+1764insTTTTTTTTTT (PRSS2) ENSP00000487822.1:n.321+1763_321+1764insTTTTTTTTTT
ENST00000634019.1:c.82+4866_82+4867insTTTTTTTTTT (PRSS2) ENSP00000488594.1:n.82+4866_82+4867insTTTTTTTTTT