Canonical Allele Identifier: CA350991866

Gene: PRSS56

Linked Data

• MyVariant Identifiers: chr2:g.233388481G>A (hg19) ; chr2:g.232523771G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232523771G>A , CM000664.2:g.232523771G>A	GRCh38
NC_000002.11:g.233388481G>A , CM000664.1:g.233388481G>A	GRCh37
NC_000002.10:g.233096725G>A	NCBI36
NG_008028.1:g.2560G>A
NG_031969.1:g.8309G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617714.2:c.1013-1G>A MANE Select	ENSP00000479745.1:n.1013-1G>A
ENST00000449534.6:c.1015G>A	ENSP00000473410.1:p.Ala339Thr
ENST00000617714.1:c.1013-1G>A	ENSP00000479745.1:n.1013-1G>A
NM_001195129.1:c.1013-1G>A	NP_001182058.1:n.1013-1G>A
NM_001195129.2:c.1013-1G>A MANE Select	NP_001182058.1:n.1013-1G>A
NM_001369848.1:c.1015G>A	NP_001356777.1:p.Ala339Thr