Canonical Allele Identifier: CA1091229270

Gene: PRSS35

Linked Data

• dbSNP Id: rs1771739615
• gnomAD v3: 6-83517220-A-G
• gnomAD v4: 6-83517220-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83517220A>G , CM000668.2:g.83517220A>G	GRCh38
NC_000006.11:g.84226939A>G , CM000668.1:g.84226939A>G	GRCh37
NC_000006.10:g.84283658A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4526A>G MANE Select	ENSP00000358714.3:n.-21+4526A>G
ENST00000369700.3:c.-21+4526A>G	ENSP00000358714.3:n.-21+4526A>G
NM_001170423.1:c.-125-4315A>G	NP_001163894.1:n.-125-4315A>G
NM_153362.2:c.-21+4526A>G	NP_699193.2:n.-21+4526A>G
NM_153362.3:c.-21+4526A>G MANE Select	NP_699193.2:n.-21+4526A>G
NM_001170423.2:c.-125-4315A>G	NP_001163894.1:n.-125-4315A>G