Canonical Allele Identifier: CA2587779595

Gene: PRSS57

Linked Data

• gnomAD v4: 19-695275-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695276_695277del , CM000681.2:g.695276_695277del	GRCh38
NC_000019.9:g.695276_695277del , CM000681.1:g.695276_695277del	GRCh37
NC_000019.8:g.646276_646277del	NCBI36
NG_051189.1:g.5255_5256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.79+75_79+76del MANE Select	ENSP00000327386.6:n.79+75_79+76del
ENST00000329267.8:c.79+75_79+76del	ENSP00000327386.6:n.79+75_79+76del
ENST00000613411.4:c.79+75_79+76del	ENSP00000482358.1:n.79+75_79+76del
NM_001308209.1:c.79+75_79+76del	NP_001295138.1:n.79+75_79+76del
NM_214710.3:c.79+75_79+76del	NP_999875.1:n.79+75_79+76del
NM_214710.4:c.79+75_79+76del	NP_999875.1:n.79+75_79+76del
NM_001308209.2:c.79+75_79+76del MANE Select	NP_001295138.2:n.79+75_79+76del
NM_214710.5:c.79+75_79+76del	NP_999875.2:n.79+75_79+76del