Canonical Allele Identifier: CA641950
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs780690327
ExAC: 1:17727688 GTCTT / G
gnomAD v2: 1-17727688-GTCTT-G
gnomAD v3: 1-17401192-GTCTT-G
gnomAD v4: 1-17401192-GTCTT-G
MyVariant Identifiers: chr1:g.17727689_17727692del (hg19) chr1:g.17401193_17401196del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401196_17401199del , CM000663.2:g.17401196_17401199del GRCh38
NC_000001.10:g.17727692_17727695del , CM000663.1:g.17727692_17727695del GRCh37
NC_000001.9:g.17600279_17600282del NCBI36
NG_032943.1:g.33951_33954del
NG_032943.2:g.33951_33954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1852-9_1852-6del MANE Select ENSP00000483125.1:n.1852-9_1852-6del
NM_207421.4:c.1852-9_1852-6del MANE Select NP_997304.3:n.1852-9_1852-6del
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