Canonical Allele Identifier: CA2587779839

Gene: PRSS57

Linked Data

• gnomAD v4: 19-695084-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695089_695090del , CM000681.2:g.695089_695090del	GRCh38
NC_000019.9:g.695089_695090del , CM000681.1:g.695089_695090del	GRCh37
NC_000019.8:g.646089_646090del	NCBI36
NG_051189.1:g.5446_5447del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-119_80-118del MANE Select	ENSP00000327386.6:n.80-119_80-118del
ENST00000329267.8:c.80-119_80-118del	ENSP00000327386.6:n.80-119_80-118del
ENST00000613411.4:c.80-116_80-115del	ENSP00000482358.1:n.80-116_80-115del
NM_001308209.1:c.80-119_80-118del	NP_001295138.1:n.80-119_80-118del
NM_214710.3:c.80-116_80-115del	NP_999875.1:n.80-116_80-115del
NM_214710.4:c.80-116_80-115del	NP_999875.1:n.80-116_80-115del
NM_001308209.2:c.80-119_80-118del MANE Select	NP_001295138.2:n.80-119_80-118del
NM_214710.5:c.80-116_80-115del	NP_999875.2:n.80-116_80-115del