Canonical Allele Identifier: CA1335307950
Gene: PRSS56 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232523523_232523524delinsCG , CM000664.2:g.232523523_232523524delinsCG GRCh38
NC_000002.11:g.233388233_233388234delinsCG , CM000664.1:g.233388233_233388234delinsCG GRCh37
NC_000002.10:g.233096477_233096478delinsCG NCBI36
NG_008028.1:g.2312_2313delinsCG
NG_031969.1:g.8061_8062delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000617714.2:c.957_958delinsCG MANE Select ENSP00000479745.1:p.Pro319=
ENST00000449534.6:c.957_958delinsCG ENSP00000473410.1:p.Pro319=
ENST00000617714.1:c.957_958delinsCG ENSP00000479745.1:p.Pro319=
NM_001195129.1:c.957_958delinsCG NP_001182058.1:p.Pro319=
NM_001195129.2:c.957_958delinsCG MANE Select NP_001182058.1:p.Pro319=
NM_001369848.1:c.957_958delinsCG NP_001356777.1:p.Pro319=