Canonical Allele Identifier: CA1642566820

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516966_83516972delinsGGGATGA , CM000668.2:g.83516966_83516972delinsGGGATGA	GRCh38
NC_000006.11:g.84226685_84226691delinsGGGATGA , CM000668.1:g.84226685_84226691delinsGGGATGA	GRCh37
NC_000006.10:g.84283404_84283410delinsGGGATGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4272_-21+4278delinsGGGATGA MANE Select	ENSP00000358714.3:n.-21+4272_-21+4278delinsGGGATGA
ENST00000369700.3:c.-21+4272_-21+4278delinsGGGATGA	ENSP00000358714.3:n.-21+4272_-21+4278delinsGGGATGA
NM_001170423.1:c.-126+4272_-126+4278delinsGGGATGA	NP_001163894.1:n.-126+4272_-126+4278delinsGGGATGA
NM_153362.2:c.-21+4272_-21+4278delinsGGGATGA	NP_699193.2:n.-21+4272_-21+4278delinsGGGATGA
NM_153362.3:c.-21+4272_-21+4278delinsGGGATGA MANE Select	NP_699193.2:n.-21+4272_-21+4278delinsGGGATGA
NM_001170423.2:c.-126+4272_-126+4278delinsGGGATGA	NP_001163894.1:n.-126+4272_-126+4278delinsGGGATGA