Canonical Allele Identifier: CA1642566787

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516888_83516889delinsAC , CM000668.2:g.83516888_83516889delinsAC	GRCh38
NC_000006.11:g.84226607_84226608delinsAC , CM000668.1:g.84226607_84226608delinsAC	GRCh37
NC_000006.10:g.84283326_84283327delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4194_-21+4195delinsAC MANE Select	ENSP00000358714.3:n.-21+4194_-21+4195delinsAC
ENST00000369700.3:c.-21+4194_-21+4195delinsAC	ENSP00000358714.3:n.-21+4194_-21+4195delinsAC
NM_001170423.1:c.-126+4194_-126+4195delinsAC	NP_001163894.1:n.-126+4194_-126+4195delinsAC
NM_153362.2:c.-21+4194_-21+4195delinsAC	NP_699193.2:n.-21+4194_-21+4195delinsAC
NM_153362.3:c.-21+4194_-21+4195delinsAC MANE Select	NP_699193.2:n.-21+4194_-21+4195delinsAC
NM_001170423.2:c.-126+4194_-126+4195delinsAC	NP_001163894.1:n.-126+4194_-126+4195delinsAC