Canonical Allele Identifier: CA2587779777

Gene: PRSS57

Linked Data

• gnomAD v4: 19-695036-G-GTCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695036_695037insTCTCT , CM000681.2:g.695036_695037insTCTCT	GRCh38
NC_000019.9:g.695036_695037insTCTCT , CM000681.1:g.695036_695037insTCTCT	GRCh37
NC_000019.8:g.646036_646037insTCTCT	NCBI36
NG_051189.1:g.5495_5496insAGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-70_80-69insAGAGA MANE Select	ENSP00000327386.6:n.80-70_80-69insAGAGA
ENST00000329267.8:c.80-70_80-69insAGAGA	ENSP00000327386.6:n.80-70_80-69insAGAGA
ENST00000613411.4:c.80-67_80-66insAGAGA	ENSP00000482358.1:n.80-67_80-66insAGAGA
NM_001308209.1:c.80-70_80-69insAGAGA	NP_001295138.1:n.80-70_80-69insAGAGA
NM_214710.3:c.80-67_80-66insAGAGA	NP_999875.1:n.80-67_80-66insAGAGA
NM_214710.4:c.80-67_80-66insAGAGA	NP_999875.1:n.80-67_80-66insAGAGA
NM_001308209.2:c.80-70_80-69insAGAGA MANE Select	NP_001295138.2:n.80-70_80-69insAGAGA
NM_214710.5:c.80-67_80-66insAGAGA	NP_999875.2:n.80-67_80-66insAGAGA