Canonical Allele Identifier: CA1156187185

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336227_17336228delinsGT , CM000663.2:g.17336227_17336228delinsGT	GRCh38
NC_000001.10:g.17662722_17662723delinsGT , CM000663.1:g.17662722_17662723delinsGT	GRCh37
NC_000001.9:g.17535309_17535310delinsGT	NCBI36
NG_023261.2:g.33038_33039delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.408+1_408+2delinsGT MANE Select	ENSP00000364597.4:n.408+1_408+2delinsGT
NM_012387.2:c.408+1_408+2delinsGT	NP_036519.2:n.408+1_408+2delinsGT
XM_011541150.1:c.340+2218_340+2219delinsGT	XP_011539452.1:n.340+2218_340+2219delinsGT
XM_011541151.1:c.408+1_408+2delinsGT	XP_011539453.1:n.408+1_408+2delinsGT
XM_011541152.1:c.-12+1_-12+2delinsGT	XP_011539454.1:n.-12+1_-12+2delinsGT
XM_011541153.1:c.408+1_408+2delinsGT	XP_011539455.1:n.408+1_408+2delinsGT
XM_011541154.1:c.408+1_408+2delinsGT	XP_011539456.1:n.408+1_408+2delinsGT
XM_011541155.1:c.408+1_408+2delinsGT	XP_011539457.1:n.408+1_408+2delinsGT
XM_011541156.1:c.408+1_408+2delinsGT	XP_011539458.1:n.408+1_408+2delinsGT
XM_011541157.1:c.-305+1_-305+2delinsGT	XP_011539459.1:n.-305+1_-305+2delinsGT
XM_011541154.2:c.408+1_408+2delinsGT	XP_011539456.1:n.408+1_408+2delinsGT
NM_012387.3:c.408+1_408+2delinsGT MANE Select	NP_036519.2:n.408+1_408+2delinsGT