Canonical Allele Identifier: CA2317263632

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.695064_695065delinsCA , CM000681.2:g.695064_695065delinsCA	GRCh38
NC_000019.9:g.695064_695065delinsCA , CM000681.1:g.695064_695065delinsCA	GRCh37
NC_000019.8:g.646064_646065delinsCA	NCBI36
NG_051189.1:g.5467_5468delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.80-98_80-97delinsTG MANE Select	ENSP00000327386.6:n.80-98_80-97delinsTG
ENST00000329267.8:c.80-98_80-97delinsTG	ENSP00000327386.6:n.80-98_80-97delinsTG
ENST00000613411.4:c.80-95_80-94delinsTG	ENSP00000482358.1:n.80-95_80-94delinsTG
NM_001308209.1:c.80-98_80-97delinsTG	NP_001295138.1:n.80-98_80-97delinsTG
NM_214710.3:c.80-95_80-94delinsTG	NP_999875.1:n.80-95_80-94delinsTG
NM_214710.4:c.80-95_80-94delinsTG	NP_999875.1:n.80-95_80-94delinsTG
NM_001308209.2:c.80-98_80-97delinsTG MANE Select	NP_001295138.2:n.80-98_80-97delinsTG
NM_214710.5:c.80-95_80-94delinsTG	NP_999875.2:n.80-95_80-94delinsTG