Canonical Allele Identifier: CA1642566903
Gene: PRSS35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517185T= , CM000668.2:g.83517185T= GRCh38
NC_000006.11:g.84226904T= , CM000668.1:g.84226904T= GRCh37
NC_000006.10:g.84283623T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4491T= MANE Select ENSP00000358714.3:n.-21+4491T=
ENST00000369700.3:c.-21+4491T= ENSP00000358714.3:n.-21+4491T=
NM_001170423.1:c.-125-4350T= NP_001163894.1:n.-125-4350T=
NM_153362.2:c.-21+4491T= NP_699193.2:n.-21+4491T=
NM_153362.3:c.-21+4491T= MANE Select NP_699193.2:n.-21+4491T=
NM_001170423.2:c.-125-4350T= NP_001163894.1:n.-125-4350T=
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