Canonical Allele Identifier: CA1642566907
Gene: PRSS35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517196_83517197delinsAT , CM000668.2:g.83517196_83517197delinsAT GRCh38
NC_000006.11:g.84226915_84226916delinsAT , CM000668.1:g.84226915_84226916delinsAT GRCh37
NC_000006.10:g.84283634_84283635delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4502_-21+4503delinsAT MANE Select ENSP00000358714.3:n.-21+4502_-21+4503delinsAT
ENST00000369700.3:c.-21+4502_-21+4503delinsAT ENSP00000358714.3:n.-21+4502_-21+4503delinsAT
NM_001170423.1:c.-125-4339_-125-4338delinsAT NP_001163894.1:n.-125-4339_-125-4338delinsAT
NM_153362.2:c.-21+4502_-21+4503delinsAT NP_699193.2:n.-21+4502_-21+4503delinsAT
NM_153362.3:c.-21+4502_-21+4503delinsAT MANE Select NP_699193.2:n.-21+4502_-21+4503delinsAT
NM_001170423.2:c.-125-4339_-125-4338delinsAT NP_001163894.1:n.-125-4339_-125-4338delinsAT