Canonical Allele Identifier: CA2317263696

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695175_695176delinsTG , CM000681.2:g.695175_695176delinsTG	GRCh38
NC_000019.9:g.695175_695176delinsTG , CM000681.1:g.695175_695176delinsTG	GRCh37
NC_000019.8:g.646175_646176delinsTG	NCBI36
NG_051189.1:g.5356_5357delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.79+176_79+177delinsCA MANE Select	ENSP00000327386.6:n.79+176_79+177delinsCA
ENST00000329267.8:c.79+176_79+177delinsCA	ENSP00000327386.6:n.79+176_79+177delinsCA
ENST00000613411.4:c.79+176_79+177delinsCA	ENSP00000482358.1:n.79+176_79+177delinsCA
NM_001308209.1:c.79+176_79+177delinsCA	NP_001295138.1:n.79+176_79+177delinsCA
NM_214710.3:c.79+176_79+177delinsCA	NP_999875.1:n.79+176_79+177delinsCA
NM_214710.4:c.79+176_79+177delinsCA	NP_999875.1:n.79+176_79+177delinsCA
NM_001308209.2:c.79+176_79+177delinsCA MANE Select	NP_001295138.2:n.79+176_79+177delinsCA
NM_214710.5:c.79+176_79+177delinsCA	NP_999875.2:n.79+176_79+177delinsCA