Canonical Allele Identifier: CA568294576
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs70987760
gnomAD v2: 6-84226294-C-CAA
gnomAD v3: 6-83516575-C-CAA
gnomAD v4: 6-83516575-C-CAA
MyVariant Identifiers: chr6:g.84226297_84226298insAA (hg19) chr6:g.84226294_84226295insAA (hg19) chr6:g.83516578_83516579insAA (hg38) chr6:g.83516575_83516576insAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516594_83516595dup , CM000668.2:g.83516594_83516595dup GRCh38
NC_000006.11:g.84226313_84226314dup , CM000668.1:g.84226313_84226314dup GRCh37
NC_000006.10:g.84283032_84283033dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3900_-21+3901dup MANE Select ENSP00000358714.3:n.-21+3900_-21+3901dup
ENST00000369700.3:c.-21+3900_-21+3901dup ENSP00000358714.3:n.-21+3900_-21+3901dup
NM_001170423.1:c.-126+3900_-126+3901dup NP_001163894.1:n.-126+3900_-126+3901dup
NM_153362.2:c.-21+3900_-21+3901dup NP_699193.2:n.-21+3900_-21+3901dup
NM_153362.3:c.-21+3900_-21+3901dup MANE Select NP_699193.2:n.-21+3900_-21+3901dup
NM_001170423.2:c.-126+3900_-126+3901dup NP_001163894.1:n.-126+3900_-126+3901dup
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