Canonical Allele Identifier: CA1156200051
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347966A= , CM000663.2:g.17347966A= GRCh38
NC_000001.10:g.17674461A= , CM000663.1:g.17674461A= GRCh37
NC_000001.9:g.17547048A= NCBI36
NG_023261.2:g.44777A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1073A= MANE Select ENSP00000364597.4:p.Gln358=
ENST00000468945.1:n.132A=
ENST00000487048.5:n.40A=
NM_012387.2:c.1073A= NP_036519.2:p.Gln358=
XM_011541150.1:c.887A= XP_011539452.1:p.Gln296=
XM_011541151.1:c.1073A= XP_011539453.1:p.Gln358=
XM_011541152.1:c.536A= XP_011539454.1:p.Gln179=
XM_011541153.1:c.1073A= XP_011539455.1:p.Gln358=
XM_011541154.1:c.1073A= XP_011539456.1:p.Gln358=
XM_011541155.1:c.1073A= XP_011539457.1:p.Gln358=
XM_011541156.1:c.1073A= XP_011539458.1:p.Gln358=
XM_011541157.1:c.182A= XP_011539459.1:p.Gln61=
XM_011541154.2:c.1073A= XP_011539456.1:p.Gln358=
NM_012387.3:c.1073A= MANE Select NP_036519.2:p.Gln358=