Canonical Allele Identifier: CA141911958
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs759545088
MyVariant Identifiers: chr6:g.84226817_84226818insT (hg19) chr6:g.83517098_83517099insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517099dup , CM000668.2:g.83517099dup GRCh38
NC_000006.11:g.84226818dup , CM000668.1:g.84226818dup GRCh37
NC_000006.10:g.84283537dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4405dup MANE Select ENSP00000358714.3:n.-21+4405dup
ENST00000369700.3:c.-21+4405dup ENSP00000358714.3:n.-21+4405dup
NM_001170423.1:c.-126+4405dup NP_001163894.1:n.-126+4405dup
NM_153362.2:c.-21+4405dup NP_699193.2:n.-21+4405dup
NM_153362.3:c.-21+4405dup MANE Select NP_699193.2:n.-21+4405dup
NM_001170423.2:c.-126+4405dup NP_001163894.1:n.-126+4405dup
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