Canonical Allele Identifier: CA1156185149
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs2074268128

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334202_17334203del , CM000663.2:g.17334202_17334203del GRCh38
NC_000001.10:g.17660697_17660698del , CM000663.1:g.17660697_17660698del GRCh37
NC_000001.9:g.17533284_17533285del NCBI36
NG_023261.2:g.31013_31014del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.340+193_340+194del MANE Select ENSP00000364597.4:n.340+193_340+194del
ENST00000375453.5:c.341-122_341-121del ENSP00000364602.1:n.341-122_341-121del
NM_012387.2:c.340+193_340+194del NP_036519.2:n.340+193_340+194del
XM_011541150.1:c.340+193_340+194del XP_011539452.1:n.340+193_340+194del
XM_011541151.1:c.340+193_340+194del XP_011539453.1:n.340+193_340+194del
XM_011541152.1:c.-80+193_-80+194del XP_011539454.1:n.-80+193_-80+194del
XM_011541153.1:c.340+193_340+194del XP_011539455.1:n.340+193_340+194del
XM_011541154.1:c.340+193_340+194del XP_011539456.1:n.340+193_340+194del
XM_011541155.1:c.340+193_340+194del XP_011539457.1:n.340+193_340+194del
XM_011541156.1:c.340+193_340+194del XP_011539458.1:n.340+193_340+194del
XM_011541157.1:c.-373+193_-373+194del XP_011539459.1:n.-373+193_-373+194del
XM_011541154.2:c.340+193_340+194del XP_011539456.1:n.340+193_340+194del
NM_012387.3:c.340+193_340+194del MANE Select NP_036519.2:n.340+193_340+194del