Canonical Allele Identifier: CA1642566681
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs759009230

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516729dup , CM000668.2:g.83516729dup GRCh38
NC_000006.11:g.84226448dup , CM000668.1:g.84226448dup GRCh37
NC_000006.10:g.84283167dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4035dup MANE Select ENSP00000358714.3:n.-21+4035dup
ENST00000369700.3:c.-21+4035dup ENSP00000358714.3:n.-21+4035dup
NM_001170423.1:c.-126+4035dup NP_001163894.1:n.-126+4035dup
NM_153362.2:c.-21+4035dup NP_699193.2:n.-21+4035dup
NM_153362.3:c.-21+4035dup MANE Select NP_699193.2:n.-21+4035dup
NM_001170423.2:c.-126+4035dup NP_001163894.1:n.-126+4035dup