Canonical Allele Identifier: CA568294598

Gene: PRSS35

Linked Data

• dbSNP Id: rs1367001612
• gnomAD v2: 6-84226576-A-C
• gnomAD v3: 6-83516857-A-C
• gnomAD v4: 6-83516857-A-C
• MyVariant Identifiers: chr6:g.84226576A>C (hg19) ; chr6:g.83516857A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516857A>C , CM000668.2:g.83516857A>C	GRCh38
NC_000006.11:g.84226576A>C , CM000668.1:g.84226576A>C	GRCh37
NC_000006.10:g.84283295A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4163A>C MANE Select	ENSP00000358714.3:n.-21+4163A>C
ENST00000369700.3:c.-21+4163A>C	ENSP00000358714.3:n.-21+4163A>C
NM_001170423.1:c.-126+4163A>C	NP_001163894.1:n.-126+4163A>C
NM_153362.2:c.-21+4163A>C	NP_699193.2:n.-21+4163A>C
NM_153362.3:c.-21+4163A>C MANE Select	NP_699193.2:n.-21+4163A>C
NM_001170423.2:c.-126+4163A>C	NP_001163894.1:n.-126+4163A>C