Canonical Allele Identifier: CA2317263403
Gene: PRSS57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694601_694606delinsATATGT , CM000681.2:g.694601_694606delinsATATGT GRCh38
NC_000019.9:g.694601_694606delinsATATGT , CM000681.1:g.694601_694606delinsATATGT GRCh37
NC_000019.8:g.645601_645606delinsATATGT NCBI36
NG_051189.1:g.5926_5931delinsACATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.233+208_233+213delinsACATAT MANE Select ENSP00000327386.6:n.233+208_233+213delinsACATAT
ENST00000329267.8:c.233+208_233+213delinsACATAT ENSP00000327386.6:n.233+208_233+213delinsACATAT
ENST00000613411.4:c.236+208_236+213delinsACATAT ENSP00000482358.1:n.236+208_236+213delinsACATAT
NM_001308209.1:c.233+208_233+213delinsACATAT NP_001295138.1:n.233+208_233+213delinsACATAT
NM_214710.3:c.236+208_236+213delinsACATAT NP_999875.1:n.236+208_236+213delinsACATAT
NM_214710.4:c.236+208_236+213delinsACATAT NP_999875.1:n.236+208_236+213delinsACATAT
NM_001308209.2:c.233+208_233+213delinsACATAT MANE Select NP_001295138.2:n.233+208_233+213delinsACATAT
NM_214710.5:c.236+208_236+213delinsACATAT NP_999875.2:n.236+208_236+213delinsACATAT