Canonical Allele Identifier: CA1642566898
Gene: PRSS35 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4470T= MANE Select ENSP00000358714.3:n.-21+4470T=
ENST00000369700.3:c.-21+4470T= ENSP00000358714.3:n.-21+4470T=
NM_001170423.1:c.-125-4371T= NP_001163894.1:n.-125-4371T=
NM_153362.2:c.-21+4470T= NP_699193.2:n.-21+4470T=
NM_153362.3:c.-21+4470T= MANE Select NP_699193.2:n.-21+4470T=
NM_001170423.2:c.-125-4371T= NP_001163894.1:n.-125-4371T=
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