Canonical Allele Identifier: CA1642566816
Gene: PRSS35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516960G= , CM000668.2:g.83516960G= GRCh38
NC_000006.11:g.84226679G= , CM000668.1:g.84226679G= GRCh37
NC_000006.10:g.84283398G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4266G= MANE Select ENSP00000358714.3:n.-21+4266G=
ENST00000369700.3:c.-21+4266G= ENSP00000358714.3:n.-21+4266G=
NM_001170423.1:c.-126+4266G= NP_001163894.1:n.-126+4266G=
NM_153362.2:c.-21+4266G= NP_699193.2:n.-21+4266G=
NM_153362.3:c.-21+4266G= MANE Select NP_699193.2:n.-21+4266G=
NM_001170423.2:c.-126+4266G= NP_001163894.1:n.-126+4266G=
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