Canonical Allele Identifier: CA2317263666

Gene: PRSS57

Linked Data

• dbSNP Id: rs2031754650
• gnomAD v4: 19-695121-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695127dup , CM000681.2:g.695127dup	GRCh38
NC_000019.9:g.695127dup , CM000681.1:g.695127dup	GRCh37
NC_000019.8:g.646127dup	NCBI36
NG_051189.1:g.5410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-155dup MANE Select	ENSP00000327386.6:n.80-155dup
ENST00000329267.8:c.80-155dup	ENSP00000327386.6:n.80-155dup
ENST00000613411.4:c.80-152dup	ENSP00000482358.1:n.80-152dup
NM_001308209.1:c.80-155dup	NP_001295138.1:n.80-155dup
NM_214710.3:c.80-152dup	NP_999875.1:n.80-152dup
NM_214710.4:c.80-152dup	NP_999875.1:n.80-152dup
NM_001308209.2:c.80-155dup MANE Select	NP_001295138.2:n.80-155dup
NM_214710.5:c.80-152dup	NP_999875.2:n.80-152dup