Canonical Allele Identifier: CA2712203564

Gene: PRSS35

Linked Data

• dbSNP Id: rs2127712928

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83517137del , CM000668.2:g.83517137del	GRCh38
NC_000006.11:g.84226856del , CM000668.1:g.84226856del	GRCh37
NC_000006.10:g.84283575del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4443del MANE Select	ENSP00000358714.3:n.-21+4443del
ENST00000369700.3:c.-21+4443del	ENSP00000358714.3:n.-21+4443del
NM_001170423.1:c.-125-4398del	NP_001163894.1:n.-125-4398del
NM_153362.2:c.-21+4443del	NP_699193.2:n.-21+4443del
NM_153362.3:c.-21+4443del MANE Select	NP_699193.2:n.-21+4443del
NM_001170423.2:c.-125-4398del	NP_001163894.1:n.-125-4398del