Canonical Allele Identifier: CA2587779871
Gene: PRSS57 HGNC NCBI

Linked Data

gnomAD v4: 19-695105-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.695105G>C , CM000681.2:g.695105G>C GRCh38
NC_000019.9:g.695105G>C , CM000681.1:g.695105G>C GRCh37
NC_000019.8:g.646105G>C NCBI36
NG_051189.1:g.5427C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.80-138C>G MANE Select ENSP00000327386.6:n.80-138C>G
ENST00000329267.8:c.80-138C>G ENSP00000327386.6:n.80-138C>G
ENST00000613411.4:c.80-135C>G ENSP00000482358.1:n.80-135C>G
NM_001308209.1:c.80-138C>G NP_001295138.1:n.80-138C>G
NM_214710.3:c.80-135C>G NP_999875.1:n.80-135C>G
NM_214710.4:c.80-135C>G NP_999875.1:n.80-135C>G
NM_001308209.2:c.80-138C>G MANE Select NP_001295138.2:n.80-138C>G
NM_214710.5:c.80-135C>G NP_999875.2:n.80-135C>G
Search 100 bp 5'
Search 100 bp 3'