Canonical Allele Identifier: CA2771946723

Gene: PRSS35

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83517187T>C , CM000668.2:g.83517187T>C	GRCh38
NC_000006.11:g.84226906T>C , CM000668.1:g.84226906T>C	GRCh37
NC_000006.10:g.84283625T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369700.4:c.-21+4493T>C MANE Select	ENSP00000358714.3:n.-21+4493T>C
ENST00000369700.3:c.-21+4493T>C	ENSP00000358714.3:n.-21+4493T>C
NM_001170423.1:c.-125-4348T>C	NP_001163894.1:n.-125-4348T>C
NM_153362.2:c.-21+4493T>C	NP_699193.2:n.-21+4493T>C
NM_153362.3:c.-21+4493T>C MANE Select	NP_699193.2:n.-21+4493T>C
NM_001170423.2:c.-125-4348T>C	NP_001163894.1:n.-125-4348T>C