Canonical Allele Identifier: CA402894588

Gene: PRSS57

Linked Data

• MyVariant Identifiers: chr19:g.694884G>C (hg19) ; chr19:g.694884G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694884G>C , CM000681.2:g.694884G>C	GRCh38
NC_000019.9:g.694884G>C , CM000681.1:g.694884G>C	GRCh37
NC_000019.8:g.645884G>C	NCBI36
NG_051189.1:g.5648C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.163C>G MANE Select	ENSP00000327386.6:p.Gln55Glu
ENST00000329267.8:c.163C>G	ENSP00000327386.6:p.Gln55Glu
ENST00000613411.4:c.166C>G	ENSP00000482358.1:p.Gln56Glu
NM_001308209.1:c.163C>G	NP_001295138.1:p.Gln55Glu
NM_214710.3:c.166C>G	NP_999875.1:p.Gln56Glu
NM_214710.4:c.166C>G	NP_999875.1:p.Gln56Glu
NM_001308209.2:c.163C>G MANE Select	NP_001295138.2:p.Gln55Glu
NM_214710.5:c.166C>G	NP_999875.2:p.Gln56Glu