Canonical Allele Identifier: CA1156200093

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347984_17347985delinsTG , CM000663.2:g.17347984_17347985delinsTG	GRCh38
NC_000001.10:g.17674479_17674480delinsTG , CM000663.1:g.17674479_17674480delinsTG	GRCh37
NC_000001.9:g.17547066_17547067delinsTG	NCBI36
NG_023261.2:g.44795_44796delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1091_1092delinsTG MANE Select	ENSP00000364597.4:p.Leu364=
ENST00000468945.1:n.150_151delinsTG
ENST00000487048.5:n.58_59delinsTG
NM_012387.2:c.1091_1092delinsTG	NP_036519.2:p.Leu364=
XM_011541150.1:c.905_906delinsTG	XP_011539452.1:p.Leu302=
XM_011541151.1:c.1091_1092delinsTG	XP_011539453.1:p.Leu364=
XM_011541152.1:c.554_555delinsTG	XP_011539454.1:p.Leu185=
XM_011541153.1:c.1091_1092delinsTG	XP_011539455.1:p.Leu364=
XM_011541154.1:c.1091_1092delinsTG	XP_011539456.1:p.Leu364=
XM_011541155.1:c.1091_1092delinsTG	XP_011539457.1:p.Leu364=
XM_011541156.1:c.1091_1092delinsTG	XP_011539458.1:p.Leu364=
XM_011541157.1:c.200_201delinsTG	XP_011539459.1:p.Leu67=
XM_011541154.2:c.1091_1092delinsTG	XP_011539456.1:p.Leu364=
NM_012387.3:c.1091_1092delinsTG MANE Select	NP_036519.2:p.Leu364=