Canonical Allele Identifier: CA2216902911

Gene: PRSS8

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31133898C>G , CM000678.2:g.31133898C>G	GRCh38
NC_000016.9:g.31145219C>G , CM000678.1:g.31145219C>G	GRCh37
NC_000016.8:g.31052720C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317508.11:c.104-510G>C MANE Select	ENSP00000319730.6:n.104-510G>C
ENST00000317508.10:c.104-510G>C	ENSP00000319730.6:n.104-510G>C
ENST00000564025.1:n.333-510G>C
ENST00000567531.5:c.104-510G>C	ENSP00000457673.1:n.104-510G>C
ENST00000567797.1:c.86-510G>C	ENSP00000458056.1:n.86-510G>C
ENST00000568261.5:c.104-510G>C	ENSP00000457750.1:n.104-510G>C
NM_002773.3:c.104-510G>C	NP_002764.1:n.104-510G>C
NM_002773.4:c.104-510G>C	NP_002764.1:n.104-510G>C
NM_002773.5:c.104-510G>C MANE Select	NP_002764.1:n.104-510G>C