Canonical Allele Identifier: CA1156198071
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17346238C= , CM000663.2:g.17346238C= GRCh38
NC_000001.10:g.17672733C= , CM000663.1:g.17672733C= GRCh37
NC_000001.9:g.17545320C= NCBI36
NG_023261.2:g.43049C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.1047+99C= MANE Select ENSP00000364597.4:n.1047+99C=
ENST00000468945.1:n.106+99C=
NM_012387.2:c.1047+99C= NP_036519.2:n.1047+99C=
XM_011541150.1:c.861+99C= XP_011539452.1:n.861+99C=
XM_011541151.1:c.1047+99C= XP_011539453.1:n.1047+99C=
XM_011541152.1:c.510+99C= XP_011539454.1:n.510+99C=
XM_011541153.1:c.1047+99C= XP_011539455.1:n.1047+99C=
XM_011541154.1:c.1047+99C= XP_011539456.1:n.1047+99C=
XM_011541155.1:c.1047+99C= XP_011539457.1:n.1047+99C=
XM_011541156.1:c.1047+99C= XP_011539458.1:n.1047+99C=
XM_011541157.1:c.156+99C= XP_011539459.1:n.156+99C=
XM_011541154.2:c.1047+99C= XP_011539456.1:n.1047+99C=
NM_012387.3:c.1047+99C= MANE Select NP_036519.2:n.1047+99C=