Canonical Allele Identifier: CA1642566627

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516620_83516622delinsTTC , CM000668.2:g.83516620_83516622delinsTTC	GRCh38
NC_000006.11:g.84226339_84226341delinsTTC , CM000668.1:g.84226339_84226341delinsTTC	GRCh37
NC_000006.10:g.84283058_84283060delinsTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+3926_-21+3928delinsTTC MANE Select	ENSP00000358714.3:n.-21+3926_-21+3928delinsTTC
ENST00000369700.3:c.-21+3926_-21+3928delinsTTC	ENSP00000358714.3:n.-21+3926_-21+3928delinsTTC
NM_001170423.1:c.-126+3926_-126+3928delinsTTC	NP_001163894.1:n.-126+3926_-126+3928delinsTTC
NM_153362.2:c.-21+3926_-21+3928delinsTTC	NP_699193.2:n.-21+3926_-21+3928delinsTTC
NM_153362.3:c.-21+3926_-21+3928delinsTTC MANE Select	NP_699193.2:n.-21+3926_-21+3928delinsTTC
NM_001170423.2:c.-126+3926_-126+3928delinsTTC	NP_001163894.1:n.-126+3926_-126+3928delinsTTC