Canonical Allele Identifier: CA303954026

Gene: PRSS57

Linked Data

• dbSNP Id: rs977798439
• gnomAD v3: 19-695145-C-A
• gnomAD v4: 19-695145-C-A
• MyVariant Identifiers: chr19:g.695145C>A (hg19) ; chr19:g.695145C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695145C>A , CM000681.2:g.695145C>A	GRCh38
NC_000019.9:g.695145C>A , CM000681.1:g.695145C>A	GRCh37
NC_000019.8:g.646145C>A	NCBI36
NG_051189.1:g.5387G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-178G>T MANE Select	ENSP00000327386.6:n.80-178G>T
ENST00000329267.8:c.80-178G>T	ENSP00000327386.6:n.80-178G>T
ENST00000613411.4:c.80-175G>T	ENSP00000482358.1:n.80-175G>T
NM_001308209.1:c.80-178G>T	NP_001295138.1:n.80-178G>T
NM_214710.3:c.80-175G>T	NP_999875.1:n.80-175G>T
NM_214710.4:c.80-175G>T	NP_999875.1:n.80-175G>T
NM_001308209.2:c.80-178G>T MANE Select	NP_001295138.2:n.80-178G>T
NM_214710.5:c.80-175G>T	NP_999875.2:n.80-175G>T