Canonical Allele Identifier: CA828897270

Gene: PRSS35

Linked Data

• dbSNP Id: rs1396505004
• gnomAD v3: 6-83516592-A-AG
• gnomAD v4: 6-83516592-A-AG
• MyVariant Identifiers: chr6:g.84226311_84226312insG (hg19) ; chr6:g.83516592_83516593insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516592_83516593insG , CM000668.2:g.83516592_83516593insG	GRCh38
NC_000006.11:g.84226311_84226312insG , CM000668.1:g.84226311_84226312insG	GRCh37
NC_000006.10:g.84283030_84283031insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+3898_-21+3899insG MANE Select	ENSP00000358714.3:n.-21+3898_-21+3899insG
ENST00000369700.3:c.-21+3898_-21+3899insG	ENSP00000358714.3:n.-21+3898_-21+3899insG
NM_001170423.1:c.-126+3898_-126+3899insG	NP_001163894.1:n.-126+3898_-126+3899insG
NM_153362.2:c.-21+3898_-21+3899insG	NP_699193.2:n.-21+3898_-21+3899insG
NM_153362.3:c.-21+3898_-21+3899insG MANE Select	NP_699193.2:n.-21+3898_-21+3899insG
NM_001170423.2:c.-126+3898_-126+3899insG	NP_001163894.1:n.-126+3898_-126+3899insG