Canonical Allele Identifier: CA2317263579

Gene: PRSS57

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694878G= , CM000681.2:g.694878G=	GRCh38
NC_000019.9:g.694878G= , CM000681.1:g.694878G=	GRCh37
NC_000019.8:g.645878G=	NCBI36
NG_051189.1:g.5654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.169C= MANE Select	ENSP00000327386.6:p.His57=
ENST00000329267.8:c.169C=	ENSP00000327386.6:p.His57=
ENST00000613411.4:c.172C=	ENSP00000482358.1:p.His58=
NM_001308209.1:c.169C=	NP_001295138.1:p.His57=
NM_214710.3:c.172C=	NP_999875.1:p.His58=
NM_214710.4:c.172C=	NP_999875.1:p.His58=
NM_001308209.2:c.169C= MANE Select	NP_001295138.2:p.His57=
NM_214710.5:c.172C=	NP_999875.2:p.His58=