Canonical Allele Identifier: CA1156184986
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs2074263836

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334012_17334015del , CM000663.2:g.17334012_17334015del GRCh38
NC_000001.10:g.17660507_17660510del , CM000663.1:g.17660507_17660510del GRCh37
NC_000001.9:g.17533094_17533097del NCBI36
NG_023261.2:g.30823_30826del

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.340+3_340+6del MANE Select ENSP00000364597.4:n.340+3_340+6del
ENST00000375453.5:c.340+3_340+6del ENSP00000364602.1:n.340+3_340+6del
NM_012387.2:c.340+3_340+6del NP_036519.2:n.340+3_340+6del
XM_011541150.1:c.340+3_340+6del XP_011539452.1:n.340+3_340+6del
XM_011541151.1:c.340+3_340+6del XP_011539453.1:n.340+3_340+6del
XM_011541152.1:c.-80+3_-80+6del XP_011539454.1:n.-80+3_-80+6del
XM_011541153.1:c.340+3_340+6del XP_011539455.1:n.340+3_340+6del
XM_011541154.1:c.340+3_340+6del XP_011539456.1:n.340+3_340+6del
XM_011541155.1:c.340+3_340+6del XP_011539457.1:n.340+3_340+6del
XM_011541156.1:c.340+3_340+6del XP_011539458.1:n.340+3_340+6del
XM_011541157.1:c.-373+3_-373+6del XP_011539459.1:n.-373+3_-373+6del
XM_011541154.2:c.340+3_340+6del XP_011539456.1:n.340+3_340+6del
NM_012387.3:c.340+3_340+6del MANE Select NP_036519.2:n.340+3_340+6del