Canonical Allele Identifier: CA1043463051
Gene: PRSS56 HGNC NCBI

Linked Data

dbSNP Id: rs1691336242
gnomAD v3: 2-232523750-AC-A
gnomAD v4: 2-232523750-AC-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1013-18del MANE Select ENSP00000479745.1:n.1013-18del
ENST00000449534.6:c.1013-15del ENSP00000473410.1:n.1013-15del
ENST00000617714.1:c.1013-18del ENSP00000479745.1:n.1013-18del
NM_001195129.1:c.1013-18del NP_001182058.1:n.1013-18del
NM_001195129.2:c.1013-18del MANE Select NP_001182058.1:n.1013-18del
NM_001369848.1:c.1013-15del NP_001356777.1:n.1013-15del
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Search 100 bp 3'