Canonical Allele Identifier: CA1335307919
Gene: PRSS56 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523455C= , CM000664.2:g.232523455C= GRCh38
NC_000002.11:g.233388165C= , CM000664.1:g.233388165C= GRCh37
NC_000002.10:g.233096409C= NCBI36
NG_008028.1:g.2244C=
NG_031969.1:g.7993C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.889C= MANE Select ENSP00000479745.1:p.Pro297=
ENST00000449534.6:c.889C= ENSP00000473410.1:p.Pro297=
ENST00000617714.1:c.889C= ENSP00000479745.1:p.Pro297=
NM_001195129.1:c.889C= NP_001182058.1:p.Pro297=
NM_001195129.2:c.889C= MANE Select NP_001182058.1:p.Pro297=
NM_001369848.1:c.889C= NP_001356777.1:p.Pro297=
Search 100 bp 5'
Search 100 bp 3'