Canonical Allele Identifier: CA402894728
Gene: PRSS57 HGNC NCBI

Linked Data

dbSNP Id: rs1599121013

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.694931A>C , CM000681.2:g.694931A>C GRCh38
NC_000019.9:g.694931A>C , CM000681.1:g.694931A>C GRCh37
NC_000019.8:g.645931A>C NCBI36
NG_051189.1:g.5601T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329267.9:c.116T>G MANE Select ENSP00000327386.6:p.Val39Gly
ENST00000329267.8:c.116T>G ENSP00000327386.6:p.Val39Gly
ENST00000613411.4:c.119T>G ENSP00000482358.1:p.Val40Gly
NM_001308209.1:c.116T>G NP_001295138.1:p.Val39Gly
NM_214710.3:c.119T>G NP_999875.1:p.Val40Gly
NM_214710.4:c.119T>G NP_999875.1:p.Val40Gly
NM_001308209.2:c.116T>G MANE Select NP_001295138.2:p.Val39Gly
NM_214710.5:c.119T>G NP_999875.2:p.Val40Gly