Canonical Allele Identifier: CA1748623991

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142752214_142752215delinsGA , CM000669.2:g.142752214_142752215delinsGA GRCh38
NC_000007.13:g.142460065_142460066delinsGA , CM000669.1:g.142460065_142460066delinsGA GRCh37
NC_000007.12:g.142139639_142139640delinsGA NCBI36
NG_008307.3:g.7731_7732delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.454+187_454+188delinsGA (PRSS1) MANE Select ENSP00000308720.7:n.454+187_454+188delinsGA
ENST00000311737.11:c.454+187_454+188delinsGA (PRSS1) ENSP00000308720.7:n.454+187_454+188delinsGA
ENST00000463701.1:n.918+187_918+188delinsGA (PRSS1)
ENST00000486171.5:c.496+187_496+188delinsGA (PRSS1) ENSP00000417854.1:n.496+187_496+188delinsGA
ENST00000492062.1:c.304+187_304+188delinsGA (PRSS1) ENSP00000419912.1:n.304+187_304+188delinsGA
ENST00000610416.2:c.370+31028_370+31029delinsGA (TRBC1) ENSP00000482915.1:n.370+31028_370+31029delinsGA
ENST00000612126.4:c.454+187_454+188delinsGA (PRSS1) ENSP00000479959.1:n.454+187_454+188delinsGA
ENST00000619214.4:c.424+187_424+188delinsGA (PRSS1) ENSP00000481361.1:n.424+187_424+188delinsGA
ENST00000633114.1:c.321+320_321+321delinsGA (PRSS2) ENSP00000487822.1:n.321+320_321+321delinsGA
ENST00000634019.1:c.82+3423_82+3424delinsGA (PRSS2) ENSP00000488594.1:n.82+3423_82+3424delinsGA
NM_002769.4:c.454+187_454+188delinsGA (PRSS1) NP_002760.1:n.454+187_454+188delinsGA
XM_011516411.1:c.1129+187_1129+188delinsGA (PRSS1) XP_011514713.1:n.1129+187_1129+188delinsGA
NM_002769.5:c.454+187_454+188delinsGA (PRSS1) MANE Select NP_002760.1:n.454+187_454+188delinsGA
NR_172947.1:n.396+187_396+188delinsGA (PRSS1)
NR_172948.1:n.393+187_393+188delinsGA (PRSS1)
NR_172949.1:n.393+187_393+188delinsGA (PRSS1)
NR_172950.1:n.307+187_307+188delinsGA (PRSS1)
NR_172951.1:n.241+187_241+188delinsGA (PRSS1)