Canonical Allele Identifier: CA884127959

Gene: PRSS57

Linked Data

• dbSNP Id: rs1315619332
• gnomAD v3: 19-695023-T-TGGGGTCA
• gnomAD v4: 19-695023-T-TGGGGTCA
• MyVariant Identifiers: chr19:g.695023_695024insGGGGTCA (hg19) ; chr19:g.695023_695024insGGGGTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695027_695033dup , CM000681.2:g.695027_695033dup	GRCh38
NC_000019.9:g.695027_695033dup , CM000681.1:g.695027_695033dup	GRCh37
NC_000019.8:g.646027_646033dup	NCBI36
NG_051189.1:g.5502_5508dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-63_80-57dup MANE Select	ENSP00000327386.6:n.80-63_80-57dup
ENST00000329267.8:c.80-63_80-57dup	ENSP00000327386.6:n.80-63_80-57dup
ENST00000613411.4:c.80-60_80-54dup	ENSP00000482358.1:n.80-60_80-54dup
NM_001308209.1:c.80-63_80-57dup	NP_001295138.1:n.80-63_80-57dup
NM_214710.3:c.80-60_80-54dup	NP_999875.1:n.80-60_80-54dup
NM_214710.4:c.80-60_80-54dup	NP_999875.1:n.80-60_80-54dup
NM_001308209.2:c.80-63_80-57dup MANE Select	NP_001295138.2:n.80-63_80-57dup
NM_214710.5:c.80-60_80-54dup	NP_999875.2:n.80-60_80-54dup