Canonical Allele Identifier: CA2317263176

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695008_695015delinsAACGGATG , CM000681.2:g.695008_695015delinsAACGGATG	GRCh38
NC_000019.9:g.695008_695015delinsAACGGATG , CM000681.1:g.695008_695015delinsAACGGATG	GRCh37
NC_000019.8:g.646008_646015delinsAACGGATG	NCBI36
NG_051189.1:g.5517_5524delinsCATCCGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-48_80-41delinsCATCCGTT MANE Select	ENSP00000327386.6:n.80-48_80-41delinsCATCCGTT
ENST00000329267.8:c.80-48_80-41delinsCATCCGTT	ENSP00000327386.6:n.80-48_80-41delinsCATCCGTT
ENST00000613411.4:c.80-45_80-38delinsCATCCGTT	ENSP00000482358.1:n.80-45_80-38delinsCATCCGTT
NM_001308209.1:c.80-48_80-41delinsCATCCGTT	NP_001295138.1:n.80-48_80-41delinsCATCCGTT
NM_214710.3:c.80-45_80-38delinsCATCCGTT	NP_999875.1:n.80-45_80-38delinsCATCCGTT
NM_214710.4:c.80-45_80-38delinsCATCCGTT	NP_999875.1:n.80-45_80-38delinsCATCCGTT
NM_001308209.2:c.80-48_80-41delinsCATCCGTT MANE Select	NP_001295138.2:n.80-48_80-41delinsCATCCGTT
NM_214710.5:c.80-45_80-38delinsCATCCGTT	NP_999875.2:n.80-45_80-38delinsCATCCGTT