Canonical Allele Identifier: CA1147309442
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17346249A= , CM000663.2:g.17346249A= GRCh38
NC_000001.10:g.17672744A= , CM000663.1:g.17672744A= GRCh37
NC_000001.9:g.17545331A= NCBI36
NG_023261.2:g.43060A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.1047+110A= MANE Select ENSP00000364597.4:n.1047+110A=
ENST00000468945.1:n.106+110A=
NM_012387.2:c.1047+110A= NP_036519.2:n.1047+110A=
XM_011541150.1:c.861+110A= XP_011539452.1:n.861+110A=
XM_011541151.1:c.1047+110A= XP_011539453.1:n.1047+110A=
XM_011541152.1:c.510+110A= XP_011539454.1:n.510+110A=
XM_011541153.1:c.1047+110A= XP_011539455.1:n.1047+110A=
XM_011541154.1:c.1047+110A= XP_011539456.1:n.1047+110A=
XM_011541155.1:c.1047+110A= XP_011539457.1:n.1047+110A=
XM_011541156.1:c.1047+110A= XP_011539458.1:n.1047+110A=
XM_011541157.1:c.156+110A= XP_011539459.1:n.156+110A=
XM_011541154.2:c.1047+110A= XP_011539456.1:n.1047+110A=
NM_012387.3:c.1047+110A= MANE Select NP_036519.2:n.1047+110A=