Canonical Allele Identifier: CA1156200164

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348009_17348010delinsGA , CM000663.2:g.17348009_17348010delinsGA	GRCh38
NC_000001.10:g.17674504_17674505delinsGA , CM000663.1:g.17674504_17674505delinsGA	GRCh37
NC_000001.9:g.17547091_17547092delinsGA	NCBI36
NG_023261.2:g.44820_44821delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1116_1117delinsGA MANE Select	ENSP00000364597.4:p.Arg372=
ENST00000468945.1:n.175_176delinsGA
ENST00000487048.5:n.83_84delinsGA
NM_012387.2:c.1116_1117delinsGA	NP_036519.2:p.Arg372=
XM_011541150.1:c.930_931delinsGA	XP_011539452.1:p.Arg310=
XM_011541151.1:c.1116_1117delinsGA	XP_011539453.1:p.Arg372=
XM_011541152.1:c.579_580delinsGA	XP_011539454.1:p.Arg193=
XM_011541153.1:c.1116_1117delinsGA	XP_011539455.1:p.Arg372=
XM_011541154.1:c.1116_1117delinsGA	XP_011539456.1:p.Arg372=
XM_011541155.1:c.1116_1117delinsGA	XP_011539457.1:p.Arg372=
XM_011541156.1:c.1116_1117delinsGA	XP_011539458.1:p.Arg372=
XM_011541157.1:c.225_226delinsGA	XP_011539459.1:p.Arg75=
XM_011541154.2:c.1116_1117delinsGA	XP_011539456.1:p.Arg372=
NM_012387.3:c.1116_1117delinsGA MANE Select	NP_036519.2:p.Arg372=