Canonical Allele Identifier: CA402894606
Gene: PRSS57 HGNC NCBI

Linked Data

gnomAD v4: 19-694890-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694890C>G , CM000681.2:g.694890C>G GRCh38
NC_000019.9:g.694890C>G , CM000681.1:g.694890C>G GRCh37
NC_000019.8:g.645890C>G NCBI36
NG_051189.1:g.5642G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.157G>C MANE Select ENSP00000327386.6:p.Gly53Arg
ENST00000329267.8:c.157G>C ENSP00000327386.6:p.Gly53Arg
ENST00000613411.4:c.160G>C ENSP00000482358.1:p.Gly54Arg
NM_001308209.1:c.157G>C NP_001295138.1:p.Gly53Arg
NM_214710.3:c.160G>C NP_999875.1:p.Gly54Arg
NM_214710.4:c.160G>C NP_999875.1:p.Gly54Arg
NM_001308209.2:c.157G>C MANE Select NP_001295138.2:p.Gly53Arg
NM_214710.5:c.160G>C NP_999875.2:p.Gly54Arg