Canonical Allele Identifier: CA568294580
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1329672519
gnomAD v2: 6-84226314-AGAAAT-A
gnomAD v3: 6-83516595-AGAAAT-A
gnomAD v4: 6-83516595-AGAAAT-A
MyVariant Identifiers: chr6:g.84226315_84226319del (hg19) chr6:g.83516596_83516600del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516596_83516600del , CM000668.2:g.83516596_83516600del GRCh38
NC_000006.11:g.84226315_84226319del , CM000668.1:g.84226315_84226319del GRCh37
NC_000006.10:g.84283034_84283038del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3902_-21+3906del MANE Select ENSP00000358714.3:n.-21+3902_-21+3906del
ENST00000369700.3:c.-21+3902_-21+3906del ENSP00000358714.3:n.-21+3902_-21+3906del
NM_001170423.1:c.-126+3902_-126+3906del NP_001163894.1:n.-126+3902_-126+3906del
NM_153362.2:c.-21+3902_-21+3906del NP_699193.2:n.-21+3902_-21+3906del
NM_153362.3:c.-21+3902_-21+3906del MANE Select NP_699193.2:n.-21+3902_-21+3906del
NM_001170423.2:c.-126+3902_-126+3906del NP_001163894.1:n.-126+3902_-126+3906del
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