Canonical Allele Identifier: CA1642566678

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516724_83516725delinsCT , CM000668.2:g.83516724_83516725delinsCT	GRCh38
NC_000006.11:g.84226443_84226444delinsCT , CM000668.1:g.84226443_84226444delinsCT	GRCh37
NC_000006.10:g.84283162_84283163delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4030_-21+4031delinsCT MANE Select	ENSP00000358714.3:n.-21+4030_-21+4031delinsCT
ENST00000369700.3:c.-21+4030_-21+4031delinsCT	ENSP00000358714.3:n.-21+4030_-21+4031delinsCT
NM_001170423.1:c.-126+4030_-126+4031delinsCT	NP_001163894.1:n.-126+4030_-126+4031delinsCT
NM_153362.2:c.-21+4030_-21+4031delinsCT	NP_699193.2:n.-21+4030_-21+4031delinsCT
NM_153362.3:c.-21+4030_-21+4031delinsCT MANE Select	NP_699193.2:n.-21+4030_-21+4031delinsCT
NM_001170423.2:c.-126+4030_-126+4031delinsCT	NP_001163894.1:n.-126+4030_-126+4031delinsCT