Canonical Allele Identifier: CA1642566732

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516796_83516797delinsCT , CM000668.2:g.83516796_83516797delinsCT	GRCh38
NC_000006.11:g.84226515_84226516delinsCT , CM000668.1:g.84226515_84226516delinsCT	GRCh37
NC_000006.10:g.84283234_84283235delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369700.4:c.-21+4102_-21+4103delinsCT MANE Select	ENSP00000358714.3:n.-21+4102_-21+4103deli...
ENST00000369700.3:c.-21+4102_-21+4103delinsCT	ENSP00000358714.3:n.-21+4102_-21+4103deli...
NM_001170423.1:c.-126+4102_-126+4103delinsCT	NP_001163894.1:n.-126+4102_-126+4103delin...
NM_153362.2:c.-21+4102_-21+4103delinsCT	NP_699193.2:n.-21+4102_-21+4103delinsCT
NM_153362.3:c.-21+4102_-21+4103delinsCT MANE Select	NP_699193.2:n.-21+4102_-21+4103delinsCT
NM_001170423.2:c.-126+4102_-126+4103delinsCT	NP_001163894.1:n.-126+4102_-126+4103delin...