Canonical Allele Identifier: CA1642566801

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516929_83516934delinsCTCTTT , CM000668.2:g.83516929_83516934delinsCTCTTT	GRCh38
NC_000006.11:g.84226648_84226653delinsCTCTTT , CM000668.1:g.84226648_84226653delinsCTCTTT	GRCh37
NC_000006.10:g.84283367_84283372delinsCTCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4235_-21+4240delinsCTCTTT MANE Select	ENSP00000358714.3:n.-21+4235_-21+4240delinsCTCTTT
ENST00000369700.3:c.-21+4235_-21+4240delinsCTCTTT	ENSP00000358714.3:n.-21+4235_-21+4240delinsCTCTTT
NM_001170423.1:c.-126+4235_-126+4240delinsCTCTTT	NP_001163894.1:n.-126+4235_-126+4240delinsCTCTTT
NM_153362.2:c.-21+4235_-21+4240delinsCTCTTT	NP_699193.2:n.-21+4235_-21+4240delinsCTCTTT
NM_153362.3:c.-21+4235_-21+4240delinsCTCTTT MANE Select	NP_699193.2:n.-21+4235_-21+4240delinsCTCTTT
NM_001170423.2:c.-126+4235_-126+4240delinsCTCTTT	NP_001163894.1:n.-126+4235_-126+4240delinsCTCTTT