Canonical Allele Identifier: CA2735458057

Gene: PRSS57

Linked Data

• dbSNP Id: rs2144819346

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694576_694577insAAAAAAAAAGGT , CM000681.2:g.694576_694577insAAAAAAAAAGGT	GRCh38
NC_000019.9:g.694576_694577insAAAAAAAAAGGT , CM000681.1:g.694576_694577insAAAAAAAAAGGT	GRCh37
NC_000019.8:g.645576_645577insAAAAAAAAAGGT	NCBI36
NG_051189.1:g.5955_5956insACCTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.233+237_233+238insACCTTTTTTTTT MANE Select	ENSP00000327386.6:n.233+237_233+238insACCTTTTTTTTT
ENST00000329267.8:c.233+237_233+238insACCTTTTTTTTT	ENSP00000327386.6:n.233+237_233+238insACCTTTTTTTTT
ENST00000613411.4:c.236+237_236+238insACCTTTTTTTTT	ENSP00000482358.1:n.236+237_236+238insACCTTTTTTTTT
NM_001308209.1:c.233+237_233+238insACCTTTTTTTTT	NP_001295138.1:n.233+237_233+238insACCTTTTTTTTT
NM_214710.3:c.236+237_236+238insACCTTTTTTTTT	NP_999875.1:n.236+237_236+238insACCTTTTTTTTT
NM_214710.4:c.236+237_236+238insACCTTTTTTTTT	NP_999875.1:n.236+237_236+238insACCTTTTTTTTT
NM_001308209.2:c.233+237_233+238insACCTTTTTTTTT MANE Select	NP_001295138.2:n.233+237_233+238insACCTTTTTTTTT
NM_214710.5:c.236+237_236+238insACCTTTTTTTTT	NP_999875.2:n.236+237_236+238insACCTTTTTTTTT