Canonical Allele Identifier: CA1335308070
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523782C= , CM000664.2:g.232523782C= GRCh38
NC_000002.11:g.233388492C= , CM000664.1:g.233388492C= GRCh37
NC_000002.10:g.233096736C= NCBI36
NG_008028.1:g.2571C=
NG_031969.1:g.8320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.1023C= MANE Select ENSP00000479745.1:p.Ser341=
ENST00000449534.6:c.1026C= ENSP00000473410.1:p.Ser342=
ENST00000617714.1:c.1023C= ENSP00000479745.1:p.Ser341=
NM_001195129.1:c.1023C= NP_001182058.1:p.Ser341=
NM_001195129.2:c.1023C= MANE Select NP_001182058.1:p.Ser341=
NM_001369848.1:c.1026C= NP_001356777.1:p.Ser342=