Canonical Allele Identifier: CA2317263657

Gene: PRSS57

Linked Data

• dbSNP Id: rs2031754318

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695107_695108del , CM000681.2:g.695107_695108del	GRCh38
NC_000019.9:g.695107_695108del , CM000681.1:g.695107_695108del	GRCh37
NC_000019.8:g.646107_646108del	NCBI36
NG_051189.1:g.5425_5426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-140_80-139del MANE Select	ENSP00000327386.6:n.80-140_80-139del
ENST00000329267.8:c.80-140_80-139del	ENSP00000327386.6:n.80-140_80-139del
ENST00000613411.4:c.80-137_80-136del	ENSP00000482358.1:n.80-137_80-136del
NM_001308209.1:c.80-140_80-139del	NP_001295138.1:n.80-140_80-139del
NM_214710.3:c.80-137_80-136del	NP_999875.1:n.80-137_80-136del
NM_214710.4:c.80-137_80-136del	NP_999875.1:n.80-137_80-136del
NM_001308209.2:c.80-140_80-139del MANE Select	NP_001295138.2:n.80-140_80-139del
NM_214710.5:c.80-137_80-136del	NP_999875.2:n.80-137_80-136del