Canonical Allele Identifier: CA1335308099

Gene: PRSS56

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523850G= , CM000664.2:g.232523850G=	GRCh38
NC_000002.11:g.233388560G= , CM000664.1:g.233388560G=	GRCh37
NC_000002.10:g.233096804G=	NCBI36
NG_008028.1:g.2639G=
NG_031969.1:g.8388G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1091G= MANE Select	ENSP00000479745.1:p.Arg364=
ENST00000449534.6:c.1094G=	ENSP00000473410.1:p.Arg365=
ENST00000617714.1:c.1091G=	ENSP00000479745.1:p.Arg364=
NM_001195129.1:c.1091G=	NP_001182058.1:p.Arg364=
NM_001195129.2:c.1091G= MANE Select	NP_001182058.1:p.Arg364=
NM_001369848.1:c.1094G=	NP_001356777.1:p.Arg365=