Canonical Allele Identifier: CA1642566752
Gene: PRSS35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516830_83516833delinsCCTT , CM000668.2:g.83516830_83516833delinsCCTT GRCh38
NC_000006.11:g.84226549_84226552delinsCCTT , CM000668.1:g.84226549_84226552delinsCCTT GRCh37
NC_000006.10:g.84283268_84283271delinsCCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4136_-21+4139delinsCCTT MANE Select ENSP00000358714.3:n.-21+4136_-21+4139delinsCCTT
ENST00000369700.3:c.-21+4136_-21+4139delinsCCTT ENSP00000358714.3:n.-21+4136_-21+4139delinsCCTT
NM_001170423.1:c.-126+4136_-126+4139delinsCCTT NP_001163894.1:n.-126+4136_-126+4139delinsCCTT
NM_153362.2:c.-21+4136_-21+4139delinsCCTT NP_699193.2:n.-21+4136_-21+4139delinsCCTT
NM_153362.3:c.-21+4136_-21+4139delinsCCTT MANE Select NP_699193.2:n.-21+4136_-21+4139delinsCCTT
NM_001170423.2:c.-126+4136_-126+4139delinsCCTT NP_001163894.1:n.-126+4136_-126+4139delinsCCTT
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