Canonical Allele Identifier: CA1335308060
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523754_232523755delinsCT , CM000664.2:g.232523754_232523755delinsCT GRCh38
NC_000002.11:g.233388464_233388465delinsCT , CM000664.1:g.233388464_233388465delinsCT GRCh37
NC_000002.10:g.233096708_233096709delinsCT NCBI36
NG_008028.1:g.2543_2544delinsCT
NG_031969.1:g.8292_8293delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-18_1013-17delinsCT MANE Select ENSP00000479745.1:n.1013-18_1013-17delinsCT
ENST00000449534.6:c.1013-15_1013-14delinsCT ENSP00000473410.1:n.1013-15_1013-14delinsCT
ENST00000617714.1:c.1013-18_1013-17delinsCT ENSP00000479745.1:n.1013-18_1013-17delinsCT
NM_001195129.1:c.1013-18_1013-17delinsCT NP_001182058.1:n.1013-18_1013-17delinsCT
NM_001195129.2:c.1013-18_1013-17delinsCT MANE Select NP_001182058.1:n.1013-18_1013-17delinsCT
NM_001369848.1:c.1013-15_1013-14delinsCT NP_001356777.1:n.1013-15_1013-14delinsCT