Canonical Allele Identifier: CA141911692
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs760963411
gnomAD v2: 6-84226293-TCAA-T
gnomAD v3: 6-83516574-TCAA-T
gnomAD v4: 6-83516574-TCAA-T
MyVariant Identifiers: chr6:g.84226294_84226296del (hg19) chr6:g.83516575_83516577del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516575_83516577del , CM000668.2:g.83516575_83516577del GRCh38
NC_000006.11:g.84226294_84226296del , CM000668.1:g.84226294_84226296del GRCh37
NC_000006.10:g.84283013_84283015del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3881_-21+3883del MANE Select ENSP00000358714.3:n.-21+3881_-21+3883del
ENST00000369700.3:c.-21+3881_-21+3883del ENSP00000358714.3:n.-21+3881_-21+3883del
NM_001170423.1:c.-126+3881_-126+3883del NP_001163894.1:n.-126+3881_-126+3883del
NM_153362.2:c.-21+3881_-21+3883del NP_699193.2:n.-21+3881_-21+3883del
NM_153362.3:c.-21+3881_-21+3883del MANE Select NP_699193.2:n.-21+3881_-21+3883del
NM_001170423.2:c.-126+3881_-126+3883del NP_001163894.1:n.-126+3881_-126+3883del
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