Canonical Allele Identifier: CA1091229082

Gene: PRSS35

Linked Data

• dbSNP Id: rs1771726016
• gnomAD v3: 6-83516717-T-G
• gnomAD v4: 6-83516717-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516717T>G , CM000668.2:g.83516717T>G	GRCh38
NC_000006.11:g.84226436T>G , CM000668.1:g.84226436T>G	GRCh37
NC_000006.10:g.84283155T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4023T>G MANE Select	ENSP00000358714.3:n.-21+4023T>G
ENST00000369700.3:c.-21+4023T>G	ENSP00000358714.3:n.-21+4023T>G
NM_001170423.1:c.-126+4023T>G	NP_001163894.1:n.-126+4023T>G
NM_153362.2:c.-21+4023T>G	NP_699193.2:n.-21+4023T>G
NM_153362.3:c.-21+4023T>G MANE Select	NP_699193.2:n.-21+4023T>G
NM_001170423.2:c.-126+4023T>G	NP_001163894.1:n.-126+4023T>G