Canonical Allele Identifier: CA1156099469
Gene: PADI2 HGNC NCBI

Linked Data

dbSNP Id: rs1931822757

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118229_17118236del , CM000663.2:g.17118229_17118236del GRCh38
NC_000001.10:g.17444724_17444731del , CM000663.1:g.17444724_17444731del GRCh37
NC_000001.9:g.17317311_17317318del NCBI36
NG_033958.1:g.6218_6225del

Transcript Alleles

HGVS Amino-acid change
ENST00000375486.9:c.92+1044_92+1051del MANE Select ENSP00000364635.4:n.92+1044_92+1051del
ENST00000375481.1:c.92+1044_92+1051del ENSP00000364630.1:n.92+1044_92+1051del
ENST00000375486.8:c.92+1044_92+1051del ENSP00000364635.4:n.92+1044_92+1051del
NM_007365.2:c.92+1044_92+1051del NP_031391.2:n.92+1044_92+1051del
XM_011540549.1:c.92+1044_92+1051del XP_011538851.1:n.92+1044_92+1051del
XR_947004.1:n.4805_4812del
XR_001736944.1:n.174+1044_174+1051del
NM_007365.3:c.92+1044_92+1051del MANE Select NP_031391.2:n.92+1044_92+1051del