Canonical Allele Identifier: CA1748623548

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142751949_142751951delinsATC , CM000669.2:g.142751949_142751951delinsATC GRCh38
NC_000007.13:g.142459800_142459802delinsATC , CM000669.1:g.142459800_142459802delinsATC GRCh37
NC_000007.12:g.142139374_142139376delinsATC NCBI36
NG_008307.3:g.7466_7468delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000311737.12:c.376_378delinsATC (PRSS1) MANE Select ENSP00000308720.7:p.Ile126=
ENST00000311737.11:c.376_378delinsATC (PRSS1) ENSP00000308720.7:p.Ile126=
ENST00000463701.1:n.840_842delinsATC (PRSS1)
ENST00000485223.1:n.1374_1376delinsATC (PRSS1)
ENST00000486171.5:c.418_420delinsATC (PRSS1) ENSP00000417854.1:p.Ile140=
ENST00000492062.1:c.226_228delinsATC (PRSS1) ENSP00000419912.1:p.Ile76=
ENST00000610416.2:c.370+30763_370+30765delinsATC (TRBC1) ENSP00000482915.1:n.370+30763_370+30765delinsATC
ENST00000612126.4:c.376_378delinsATC (PRSS1) ENSP00000479959.1:p.Ile126=
ENST00000619214.4:c.346_348delinsATC (PRSS1) ENSP00000481361.1:p.Ile116=
ENST00000633114.1:c.321+55_321+57delinsATC (PRSS2) ENSP00000487822.1:n.321+55_321+57delinsATC
ENST00000634019.1:c.82+3158_82+3160delinsATC (PRSS2) ENSP00000488594.1:n.82+3158_82+3160delinsATC
NM_002769.4:c.376_378delinsATC (PRSS1) NP_002760.1:p.Ile126=
XM_011516411.1:c.1051_1053delinsATC (PRSS1) XP_011514713.1:p.Ile351=
NM_002769.5:c.376_378delinsATC (PRSS1) MANE Select NP_002760.1:p.Ile126=
NR_172947.1:n.318_320delinsATC (PRSS1)
NR_172948.1:n.315_317delinsATC (PRSS1)
NR_172949.1:n.315_317delinsATC (PRSS1)
NR_172950.1:n.229_231delinsATC (PRSS1)
NR_172951.1:n.163_165delinsATC (PRSS1)