Canonical Allele Identifier: CA2663619359
Gene: PRSS56 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523497del , CM000664.2:g.232523497del GRCh38
NC_000002.11:g.233388207del , CM000664.1:g.233388207del GRCh37
NC_000002.10:g.233096451del NCBI36
NG_008028.1:g.2286del
NG_031969.1:g.8035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.931del MANE Select ENSP00000479745.1:p.Asp311ThrfsTer26
ENST00000449534.6:c.931del ENSP00000473410.1:p.Asp311ThrfsTer26
ENST00000617714.1:c.931del ENSP00000479745.1:p.Asp311ThrfsTer26
NM_001195129.1:c.931del NP_001182058.1:p.Asp311ThrfsTer26
NM_001195129.2:c.931del MANE Select NP_001182058.1:p.Asp311ThrfsTer26
NM_001369848.1:c.931del NP_001356777.1:p.Asp311ThrfsTer26