Canonical Allele Identifier: CA1335308062

Gene: PRSS56

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523760C= , CM000664.2:g.232523760C=	GRCh38
NC_000002.11:g.233388470C= , CM000664.1:g.233388470C=	GRCh37
NC_000002.10:g.233096714C=	NCBI36
NG_008028.1:g.2549C=
NG_031969.1:g.8298C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1013-12C= MANE Select	ENSP00000479745.1:n.1013-12C=
ENST00000449534.6:c.1013-9C=	ENSP00000473410.1:n.1013-9C=
ENST00000617714.1:c.1013-12C=	ENSP00000479745.1:n.1013-12C=
NM_001195129.1:c.1013-12C=	NP_001182058.1:n.1013-12C=
NM_001195129.2:c.1013-12C= MANE Select	NP_001182058.1:n.1013-12C=
NM_001369848.1:c.1013-9C=	NP_001356777.1:n.1013-9C=