Canonical Allele Identifier: CA2754657293
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523788_232523789dup , CM000664.2:g.232523788_232523789dup GRCh38
NC_000002.11:g.233388498_233388499dup , CM000664.1:g.233388498_233388499dup GRCh37
NC_000002.10:g.233096742_233096743dup NCBI36
NG_008028.1:g.2577_2578dup
NG_031969.1:g.8326_8327dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1029_1030dup MANE Select ENSP00000479745.1:p.Pro344ArgfsTer?
ENST00000449534.6:c.1032_1033dup ENSP00000473410.1:p.Pro345ArgfsTer?
ENST00000617714.1:c.1029_1030dup ENSP00000479745.1:p.Pro344ArgfsTer?
NM_001195129.1:c.1029_1030dup NP_001182058.1:p.Pro344ArgfsTer?
NM_001195129.2:c.1029_1030dup MANE Select NP_001182058.1:p.Pro344ArgfsTer?
NM_001369848.1:c.1032_1033dup NP_001356777.1:p.Pro345ArgfsTer?