Canonical Allele Identifier: CA2701762696

Gene: PRSS56

Linked Data

• dbSNP Id: rs2106202138

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523849del , CM000664.2:g.232523849del	GRCh38
NC_000002.11:g.233388559del , CM000664.1:g.233388559del	GRCh37
NC_000002.10:g.233096803del	NCBI36
NG_008028.1:g.2638del
NG_031969.1:g.8387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1090del MANE Select	ENSP00000479745.1:p.Arg364GlyfsTer?
ENST00000449534.6:c.1093del	ENSP00000473410.1:p.Arg365GlyfsTer?
ENST00000617714.1:c.1090del	ENSP00000479745.1:p.Arg364GlyfsTer?
NM_001195129.1:c.1090del	NP_001182058.1:p.Arg364GlyfsTer?
NM_001195129.2:c.1090del MANE Select	NP_001182058.1:p.Arg364GlyfsTer?
NM_001369848.1:c.1093del	NP_001356777.1:p.Arg365GlyfsTer?