Canonical Allele Identifier: CA141912003
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs752406648
gnomAD v2: 6-84226878-CTCTA-C
gnomAD v3: 6-83517159-CTCTA-C
gnomAD v4: 6-83517159-CTCTA-C
MyVariant Identifiers: chr6:g.84226879_84226882del (hg19) chr6:g.83517160_83517163del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517164_83517167del , CM000668.2:g.83517164_83517167del GRCh38
NC_000006.11:g.84226883_84226886del , CM000668.1:g.84226883_84226886del GRCh37
NC_000006.10:g.84283602_84283605del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4470_-21+4473del MANE Select ENSP00000358714.3:n.-21+4470_-21+4473del
ENST00000369700.3:c.-21+4470_-21+4473del ENSP00000358714.3:n.-21+4470_-21+4473del
NM_001170423.1:c.-125-4371_-125-4368del NP_001163894.1:n.-125-4371_-125-4368del
NM_153362.2:c.-21+4470_-21+4473del NP_699193.2:n.-21+4470_-21+4473del
NM_153362.3:c.-21+4470_-21+4473del MANE Select NP_699193.2:n.-21+4470_-21+4473del
NM_001170423.2:c.-125-4371_-125-4368del NP_001163894.1:n.-125-4371_-125-4368del
Search 100 bp 5'
Search 100 bp 3'