Canonical Allele Identifier: CA568294614
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1335166080
gnomAD v2: 6-84226915-AT-A
gnomAD v3: 6-83517196-AT-A
gnomAD v4: 6-83517196-AT-A
MyVariant Identifiers: chr6:g.84226916del (hg19) chr6:g.83517197del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517198del , CM000668.2:g.83517198del GRCh38
NC_000006.11:g.84226917del , CM000668.1:g.84226917del GRCh37
NC_000006.10:g.84283636del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4504del MANE Select ENSP00000358714.3:n.-21+4504del
ENST00000369700.3:c.-21+4504del ENSP00000358714.3:n.-21+4504del
NM_001170423.1:c.-125-4337del NP_001163894.1:n.-125-4337del
NM_153362.2:c.-21+4504del NP_699193.2:n.-21+4504del
NM_153362.3:c.-21+4504del MANE Select NP_699193.2:n.-21+4504del
NM_001170423.2:c.-125-4337del NP_001163894.1:n.-125-4337del
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