Canonical Allele Identifier: CA1148873597

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348008_17348009delinsGG , CM000663.2:g.17348008_17348009delinsGG	GRCh38
NC_000001.10:g.17674503_17674504delinsGG , CM000663.1:g.17674503_17674504delinsGG	GRCh37
NC_000001.9:g.17547090_17547091delinsGG	NCBI36
NG_023261.2:g.44819_44820delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1115_1116delinsGG MANE Select	ENSP00000364597.4:p.Arg372=
ENST00000468945.1:n.174_175delinsGG
ENST00000487048.5:n.82_83delinsGG
NM_012387.2:c.1115_1116delinsGG	NP_036519.2:p.Arg372=
XM_011541150.1:c.929_930delinsGG	XP_011539452.1:p.Arg310=
XM_011541151.1:c.1115_1116delinsGG	XP_011539453.1:p.Arg372=
XM_011541152.1:c.578_579delinsGG	XP_011539454.1:p.Arg193=
XM_011541153.1:c.1115_1116delinsGG	XP_011539455.1:p.Arg372=
XM_011541154.1:c.1115_1116delinsGG	XP_011539456.1:p.Arg372=
XM_011541155.1:c.1115_1116delinsGG	XP_011539457.1:p.Arg372=
XM_011541156.1:c.1115_1116delinsGG	XP_011539458.1:p.Arg372=
XM_011541157.1:c.224_225delinsGG	XP_011539459.1:p.Arg75=
XM_011541154.2:c.1115_1116delinsGG	XP_011539456.1:p.Arg372=
NM_012387.3:c.1115_1116delinsGG MANE Select	NP_036519.2:p.Arg372=