Canonical Allele Identifier: CA2569493407
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347948_17347954del , CM000663.2:g.17347948_17347954del GRCh38
NC_000001.10:g.17674443_17674449del , CM000663.1:g.17674443_17674449del GRCh37
NC_000001.9:g.17547030_17547036del NCBI36
NG_023261.2:g.44759_44765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1055_1061del MANE Select ENSP00000364597.4:p.Met352ThrfsTer23
ENST00000468945.1:n.114_120del
ENST00000487048.5:n.22_28del
NM_012387.2:c.1055_1061del NP_036519.2:p.Met352ThrfsTer23
XM_011541150.1:c.869_875del XP_011539452.1:p.Met290ThrfsTer23
XM_011541151.1:c.1055_1061del XP_011539453.1:p.Met352ThrfsTer23
XM_011541152.1:c.518_524del XP_011539454.1:p.Met173ThrfsTer23
XM_011541153.1:c.1055_1061del XP_011539455.1:p.Met352ThrfsTer23
XM_011541154.1:c.1055_1061del XP_011539456.1:p.Met352ThrfsTer23
XM_011541155.1:c.1055_1061del XP_011539457.1:p.Met352ThrfsTer23
XM_011541156.1:c.1055_1061del XP_011539458.1:p.Met352ThrfsTer23
XM_011541157.1:c.164_170del XP_011539459.1:p.Met55ThrfsTer23
XM_011541154.2:c.1055_1061del XP_011539456.1:p.Met352ThrfsTer23
NM_012387.3:c.1055_1061del MANE Select NP_036519.2:p.Met352ThrfsTer23