Canonical Allele Identifier: CA1108082669

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753903_142753904insGA , CM000669.2:g.142753903_142753904insGA GRCh38
NC_000007.13:g.142461754_142461755insGA , CM000669.1:g.142461754_142461755insGA GRCh37
NC_000007.12:g.142141328_142141329insGA NCBI36
NG_008307.3:g.9420_9421insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32717_370+32718insGA (TRBC1) ENSP00000482915.1:n.370+32717_370+32718insGA
ENST00000612126.4:c.591+1336_591+1337insGA (PRSS1) ENSP00000479959.1:n.591+1336_591+1337insGA
ENST00000633114.1:c.321+2009_321+2010insGA (PRSS2) ENSP00000487822.1:n.321+2009_321+2010insGA
ENST00000634019.1:c.82+5112_82+5113insGA (PRSS2) ENSP00000488594.1:n.82+5112_82+5113insGA