Canonical Allele Identifier: CA1091229196
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1771733312
gnomAD v3: 6-83516913-A-T
gnomAD v4: 6-83516913-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516913A>T , CM000668.2:g.83516913A>T GRCh38
NC_000006.11:g.84226632A>T , CM000668.1:g.84226632A>T GRCh37
NC_000006.10:g.84283351A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4219A>T MANE Select ENSP00000358714.3:n.-21+4219A>T
ENST00000369700.3:c.-21+4219A>T ENSP00000358714.3:n.-21+4219A>T
NM_001170423.1:c.-126+4219A>T NP_001163894.1:n.-126+4219A>T
NM_153362.2:c.-21+4219A>T NP_699193.2:n.-21+4219A>T
NM_153362.3:c.-21+4219A>T MANE Select NP_699193.2:n.-21+4219A>T
NM_001170423.2:c.-126+4219A>T NP_001163894.1:n.-126+4219A>T