Canonical Allele Identifier: CA18622014
Gene: PADI2 HGNC NCBI

Linked Data

dbSNP Id: rs1020897930
MyVariant Identifiers: chr1:g.17444869del (hg19) chr1:g.17118374del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118374del , CM000663.2:g.17118374del GRCh38
NC_000001.10:g.17444869del , CM000663.1:g.17444869del GRCh37
NC_000001.9:g.17317456del NCBI36
NG_033958.1:g.6080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+906del MANE Select ENSP00000364635.4:n.92+906del
ENST00000375481.1:c.92+906del ENSP00000364630.1:n.92+906del
ENST00000375486.8:c.92+906del ENSP00000364635.4:n.92+906del
NM_007365.2:c.92+906del NP_031391.2:n.92+906del
XM_011540549.1:c.92+906del XP_011538851.1:n.92+906del
XR_947004.1:n.4950del
XR_001736944.1:n.174+906del
NM_007365.3:c.92+906del MANE Select NP_031391.2:n.92+906del
Search 100 bp 5'
Search 100 bp 3'