Canonical Allele Identifier: CA1642566788
Gene: PRSS35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516889C= , CM000668.2:g.83516889C= GRCh38
NC_000006.11:g.84226608C= , CM000668.1:g.84226608C= GRCh37
NC_000006.10:g.84283327C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4195C= MANE Select ENSP00000358714.3:n.-21+4195C=
ENST00000369700.3:c.-21+4195C= ENSP00000358714.3:n.-21+4195C=
NM_001170423.1:c.-126+4195C= NP_001163894.1:n.-126+4195C=
NM_153362.2:c.-21+4195C= NP_699193.2:n.-21+4195C=
NM_153362.3:c.-21+4195C= MANE Select NP_699193.2:n.-21+4195C=
NM_001170423.2:c.-126+4195C= NP_001163894.1:n.-126+4195C=