Canonical Allele Identifier: CA2317263406

Gene: PRSS57

Linked Data

• dbSNP Id: rs2031735727

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694605_694606dup , CM000681.2:g.694605_694606dup	GRCh38
NC_000019.9:g.694605_694606dup , CM000681.1:g.694605_694606dup	GRCh37
NC_000019.8:g.645605_645606dup	NCBI36
NG_051189.1:g.5927_5928dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.233+209_233+210dup MANE Select	ENSP00000327386.6:n.233+209_233+210dup
ENST00000329267.8:c.233+209_233+210dup	ENSP00000327386.6:n.233+209_233+210dup
ENST00000613411.4:c.236+209_236+210dup	ENSP00000482358.1:n.236+209_236+210dup
NM_001308209.1:c.233+209_233+210dup	NP_001295138.1:n.233+209_233+210dup
NM_214710.3:c.236+209_236+210dup	NP_999875.1:n.236+209_236+210dup
NM_214710.4:c.236+209_236+210dup	NP_999875.1:n.236+209_236+210dup
NM_001308209.2:c.233+209_233+210dup MANE Select	NP_001295138.2:n.233+209_233+210dup
NM_214710.5:c.236+209_236+210dup	NP_999875.2:n.236+209_236+210dup