Canonical Allele Identifier: CA1156200021
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347960_17347961delinsAC , CM000663.2:g.17347960_17347961delinsAC GRCh38
NC_000001.10:g.17674455_17674456delinsAC , CM000663.1:g.17674455_17674456delinsAC GRCh37
NC_000001.9:g.17547042_17547043delinsAC NCBI36
NG_023261.2:g.44771_44772delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1067_1068delinsAC MANE Select ENSP00000364597.4:p.Tyr356=
ENST00000468945.1:n.126_127delinsAC
ENST00000487048.5:n.34_35delinsAC
NM_012387.2:c.1067_1068delinsAC NP_036519.2:p.Tyr356=
XM_011541150.1:c.881_882delinsAC XP_011539452.1:p.Tyr294=
XM_011541151.1:c.1067_1068delinsAC XP_011539453.1:p.Tyr356=
XM_011541152.1:c.530_531delinsAC XP_011539454.1:p.Tyr177=
XM_011541153.1:c.1067_1068delinsAC XP_011539455.1:p.Tyr356=
XM_011541154.1:c.1067_1068delinsAC XP_011539456.1:p.Tyr356=
XM_011541155.1:c.1067_1068delinsAC XP_011539457.1:p.Tyr356=
XM_011541156.1:c.1067_1068delinsAC XP_011539458.1:p.Tyr356=
XM_011541157.1:c.176_177delinsAC XP_011539459.1:p.Tyr59=
XM_011541154.2:c.1067_1068delinsAC XP_011539456.1:p.Tyr356=
NM_012387.3:c.1067_1068delinsAC MANE Select NP_036519.2:p.Tyr356=