Canonical Allele Identifier: CA1156099498
Gene: PADI2 HGNC NCBI

Linked Data

dbSNP Id: rs1931824453

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118272_17118273del , CM000663.2:g.17118272_17118273del GRCh38
NC_000001.10:g.17444767_17444768del , CM000663.1:g.17444767_17444768del GRCh37
NC_000001.9:g.17317354_17317355del NCBI36
NG_033958.1:g.6181_6182del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1007_92+1008del MANE Select ENSP00000364635.4:n.92+1007_92+1008del
ENST00000375481.1:c.92+1007_92+1008del ENSP00000364630.1:n.92+1007_92+1008del
ENST00000375486.8:c.92+1007_92+1008del ENSP00000364635.4:n.92+1007_92+1008del
NM_007365.2:c.92+1007_92+1008del NP_031391.2:n.92+1007_92+1008del
XM_011540549.1:c.92+1007_92+1008del XP_011538851.1:n.92+1007_92+1008del
XR_947004.1:n.4848_4849del
XR_001736944.1:n.174+1007_174+1008del
NM_007365.3:c.92+1007_92+1008del MANE Select NP_031391.2:n.92+1007_92+1008del