Canonical Allele Identifier: CA1091228880
Gene: PRSS35 HGNC NCBI

Linked Data

gnomAD v3: 6-83516574-TCAAAA-T
gnomAD v4: 6-83516574-TCAAAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516575_83516579del , CM000668.2:g.83516575_83516579del GRCh38
NC_000006.11:g.84226294_84226298del , CM000668.1:g.84226294_84226298del GRCh37
NC_000006.10:g.84283013_84283017del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3881_-21+3885del MANE Select ENSP00000358714.3:n.-21+3881_-21+3885del
ENST00000369700.3:c.-21+3881_-21+3885del ENSP00000358714.3:n.-21+3881_-21+3885del
NM_001170423.1:c.-126+3881_-126+3885del NP_001163894.1:n.-126+3881_-126+3885del
NM_153362.2:c.-21+3881_-21+3885del NP_699193.2:n.-21+3881_-21+3885del
NM_153362.3:c.-21+3881_-21+3885del MANE Select NP_699193.2:n.-21+3881_-21+3885del
NM_001170423.2:c.-126+3881_-126+3885del NP_001163894.1:n.-126+3881_-126+3885del
Search 100 bp 5'
Search 100 bp 3'