Canonical Allele Identifier: CA1642566905

Gene: PRSS35

Linked Data

• dbSNP Id: rs767708017

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83517190A>G , CM000668.2:g.83517190A>G	GRCh38
NC_000006.11:g.84226909A>G , CM000668.1:g.84226909A>G	GRCh37
NC_000006.10:g.84283628A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4496A>G MANE Select	ENSP00000358714.3:n.-21+4496A>G
ENST00000369700.3:c.-21+4496A>G	ENSP00000358714.3:n.-21+4496A>G
NM_001170423.1:c.-125-4345A>G	NP_001163894.1:n.-125-4345A>G
NM_153362.2:c.-21+4496A>G	NP_699193.2:n.-21+4496A>G
NM_153362.3:c.-21+4496A>G MANE Select	NP_699193.2:n.-21+4496A>G
NM_001170423.2:c.-125-4345A>G	NP_001163894.1:n.-125-4345A>G