Canonical Allele Identifier: CA2317263547

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694829T= , CM000681.2:g.694829T=	GRCh38
NC_000019.9:g.694829T= , CM000681.1:g.694829T=	GRCh37
NC_000019.8:g.645829T=	NCBI36
NG_051189.1:g.5703A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.218A= MANE Select	ENSP00000327386.6:p.His73=
ENST00000329267.8:c.218A=	ENSP00000327386.6:p.His73=
ENST00000613411.4:c.221A=	ENSP00000482358.1:p.His74=
NM_001308209.1:c.218A=	NP_001295138.1:p.His73=
NM_214710.3:c.221A=	NP_999875.1:p.His74=
NM_214710.4:c.221A=	NP_999875.1:p.His74=
NM_001308209.2:c.218A= MANE Select	NP_001295138.2:p.His73=
NM_214710.5:c.221A=	NP_999875.2:p.His74=