Canonical Allele Identifier: CA1156185128
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334178C= , CM000663.2:g.17334178C= GRCh38
NC_000001.10:g.17660673C= , CM000663.1:g.17660673C= GRCh37
NC_000001.9:g.17533260C= NCBI36
NG_023261.2:g.30989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.340+169C= MANE Select ENSP00000364597.4:n.340+169C=
ENST00000375453.5:c.341-146C= ENSP00000364602.1:n.341-146C=
NM_012387.2:c.340+169C= NP_036519.2:n.340+169C=
XM_011541150.1:c.340+169C= XP_011539452.1:n.340+169C=
XM_011541151.1:c.340+169C= XP_011539453.1:n.340+169C=
XM_011541152.1:c.-80+169C= XP_011539454.1:n.-80+169C=
XM_011541153.1:c.340+169C= XP_011539455.1:n.340+169C=
XM_011541154.1:c.340+169C= XP_011539456.1:n.340+169C=
XM_011541155.1:c.340+169C= XP_011539457.1:n.340+169C=
XM_011541156.1:c.340+169C= XP_011539458.1:n.340+169C=
XM_011541157.1:c.-373+169C= XP_011539459.1:n.-373+169C=
XM_011541154.2:c.340+169C= XP_011539456.1:n.340+169C=
NM_012387.3:c.340+169C= MANE Select NP_036519.2:n.340+169C=