Canonical Allele Identifier: CA1156199983
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347950_17347951delinsGA , CM000663.2:g.17347950_17347951delinsGA GRCh38
NC_000001.10:g.17674445_17674446delinsGA , CM000663.1:g.17674445_17674446delinsGA GRCh37
NC_000001.9:g.17547032_17547033delinsGA NCBI36
NG_023261.2:g.44761_44762delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1057_1058delinsGA MANE Select ENSP00000364597.4:p.Glu353=
ENST00000468945.1:n.116_117delinsGA
ENST00000487048.5:n.24_25delinsGA
NM_012387.2:c.1057_1058delinsGA NP_036519.2:p.Glu353=
XM_011541150.1:c.871_872delinsGA XP_011539452.1:p.Glu291=
XM_011541151.1:c.1057_1058delinsGA XP_011539453.1:p.Glu353=
XM_011541152.1:c.520_521delinsGA XP_011539454.1:p.Glu174=
XM_011541153.1:c.1057_1058delinsGA XP_011539455.1:p.Glu353=
XM_011541154.1:c.1057_1058delinsGA XP_011539456.1:p.Glu353=
XM_011541155.1:c.1057_1058delinsGA XP_011539457.1:p.Glu353=
XM_011541156.1:c.1057_1058delinsGA XP_011539458.1:p.Glu353=
XM_011541157.1:c.166_167delinsGA XP_011539459.1:p.Glu56=
XM_011541154.2:c.1057_1058delinsGA XP_011539456.1:p.Glu353=
NM_012387.3:c.1057_1058delinsGA MANE Select NP_036519.2:p.Glu353=