Canonical Allele Identifier: CA1642566625
Gene: PRSS35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516618_83516619delinsTC , CM000668.2:g.83516618_83516619delinsTC GRCh38
NC_000006.11:g.84226337_84226338delinsTC , CM000668.1:g.84226337_84226338delinsTC GRCh37
NC_000006.10:g.84283056_84283057delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3924_-21+3925delinsTC MANE Select ENSP00000358714.3:n.-21+3924_-21+3925delinsTC
ENST00000369700.3:c.-21+3924_-21+3925delinsTC ENSP00000358714.3:n.-21+3924_-21+3925delinsTC
NM_001170423.1:c.-126+3924_-126+3925delinsTC NP_001163894.1:n.-126+3924_-126+3925delinsTC
NM_153362.2:c.-21+3924_-21+3925delinsTC NP_699193.2:n.-21+3924_-21+3925delinsTC
NM_153362.3:c.-21+3924_-21+3925delinsTC MANE Select NP_699193.2:n.-21+3924_-21+3925delinsTC
NM_001170423.2:c.-126+3924_-126+3925delinsTC NP_001163894.1:n.-126+3924_-126+3925delinsTC