Canonical Allele Identifier: CA884127979

Gene: PRSS57

Linked Data

• dbSNP Id: rs1193202032
• gnomAD v3: 19-695035-AG-A
• gnomAD v4: 19-695035-AG-A
• MyVariant Identifiers: chr19:g.695036del (hg19) ; chr19:g.695036del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695040del , CM000681.2:g.695040del	GRCh38
NC_000019.9:g.695040del , CM000681.1:g.695040del	GRCh37
NC_000019.8:g.646040del	NCBI36
NG_051189.1:g.5496del

Transcript Alleles

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