Canonical Allele Identifier: CA828897238

Gene: PRSS35

Linked Data

• dbSNP Id: rs70987760
• gnomAD v3: 6-83516575-CAAAAAAAA-C
• gnomAD v4: 6-83516575-CAAAAAAAA-C
• MyVariant Identifiers: chr6:g.84226295_84226302del (hg19) ; chr6:g.83516576_83516583del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516588_83516595del , CM000668.2:g.83516588_83516595del	GRCh38
NC_000006.11:g.84226307_84226314del , CM000668.1:g.84226307_84226314del	GRCh37
NC_000006.10:g.84283026_84283033del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+3894_-21+3901del MANE Select	ENSP00000358714.3:n.-21+3894_-21+3901del
ENST00000369700.3:c.-21+3894_-21+3901del	ENSP00000358714.3:n.-21+3894_-21+3901del
NM_001170423.1:c.-126+3894_-126+3901del	NP_001163894.1:n.-126+3894_-126+3901del
NM_153362.2:c.-21+3894_-21+3901del	NP_699193.2:n.-21+3894_-21+3901del
NM_153362.3:c.-21+3894_-21+3901del MANE Select	NP_699193.2:n.-21+3894_-21+3901del
NM_001170423.2:c.-126+3894_-126+3901del	NP_001163894.1:n.-126+3894_-126+3901del