Canonical Allele Identifier: CA1642566592

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516574_83516577delinsTCAA , CM000668.2:g.83516574_83516577delinsTCAA	GRCh38
NC_000006.11:g.84226293_84226296delinsTCAA , CM000668.1:g.84226293_84226296delinsTCAA	GRCh37
NC_000006.10:g.84283012_84283015delinsTCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+3880_-21+3883delinsTCAA MANE Select	ENSP00000358714.3:n.-21+3880_-21+3883delinsTCAA
ENST00000369700.3:c.-21+3880_-21+3883delinsTCAA	ENSP00000358714.3:n.-21+3880_-21+3883delinsTCAA
NM_001170423.1:c.-126+3880_-126+3883delinsTCAA	NP_001163894.1:n.-126+3880_-126+3883delinsTCAA
NM_153362.2:c.-21+3880_-21+3883delinsTCAA	NP_699193.2:n.-21+3880_-21+3883delinsTCAA
NM_153362.3:c.-21+3880_-21+3883delinsTCAA MANE Select	NP_699193.2:n.-21+3880_-21+3883delinsTCAA
NM_001170423.2:c.-126+3880_-126+3883delinsTCAA	NP_001163894.1:n.-126+3880_-126+3883delinsTCAA