Canonical Allele Identifier: CA2546353358

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142753791_142753792insG , CM000669.2:g.142753791_142753792insG GRCh38
NC_000007.13:g.142461642_142461643insG , CM000669.1:g.142461642_142461643insG GRCh37
NC_000007.12:g.142141216_142141217insG NCBI36
NG_008307.3:g.9308_9309insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000610416.2:c.370+32605_370+32606insG (TRBC1) ENSP00000482915.1:n.370+32605_370+32606insG
ENST00000612126.4:c.591+1224_591+1225insG (PRSS1) ENSP00000479959.1:n.591+1224_591+1225insG
ENST00000633114.1:c.321+1897_321+1898insG (PRSS2) ENSP00000487822.1:n.321+1897_321+1898insG
ENST00000634019.1:c.82+5000_82+5001insG (PRSS2) ENSP00000488594.1:n.82+5000_82+5001insG