Canonical Allele Identifier: CA2317263734

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695253_695255delinsGCT , CM000681.2:g.695253_695255delinsGCT	GRCh38
NC_000019.9:g.695253_695255delinsGCT , CM000681.1:g.695253_695255delinsGCT	GRCh37
NC_000019.8:g.646253_646255delinsGCT	NCBI36
NG_051189.1:g.5277_5279delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.79+97_79+99delinsAGC MANE Select	ENSP00000327386.6:n.79+97_79+99delinsAGC
ENST00000329267.8:c.79+97_79+99delinsAGC	ENSP00000327386.6:n.79+97_79+99delinsAGC
ENST00000613411.4:c.79+97_79+99delinsAGC	ENSP00000482358.1:n.79+97_79+99delinsAGC
NM_001308209.1:c.79+97_79+99delinsAGC	NP_001295138.1:n.79+97_79+99delinsAGC
NM_214710.3:c.79+97_79+99delinsAGC	NP_999875.1:n.79+97_79+99delinsAGC
NM_214710.4:c.79+97_79+99delinsAGC	NP_999875.1:n.79+97_79+99delinsAGC
NM_001308209.2:c.79+97_79+99delinsAGC MANE Select	NP_001295138.2:n.79+97_79+99delinsAGC
NM_214710.5:c.79+97_79+99delinsAGC	NP_999875.2:n.79+97_79+99delinsAGC