Canonical Allele Identifier: CA1156187323

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336333_17336335delinsCTG , CM000663.2:g.17336333_17336335delinsCTG	GRCh38
NC_000001.10:g.17662828_17662830delinsCTG , CM000663.1:g.17662828_17662830delinsCTG	GRCh37
NC_000001.9:g.17535415_17535417delinsCTG	NCBI36
NG_023261.2:g.33144_33146delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.408+107_408+109delinsCTG MANE Select	ENSP00000364597.4:n.408+107_408+109delinsCTG
NM_012387.2:c.408+107_408+109delinsCTG	NP_036519.2:n.408+107_408+109delinsCTG
XM_011541150.1:c.340+2324_340+2326delinsCTG	XP_011539452.1:n.340+2324_340+2326delinsCTG
XM_011541151.1:c.408+107_408+109delinsCTG	XP_011539453.1:n.408+107_408+109delinsCTG
XM_011541152.1:c.-12+107_-12+109delinsCTG	XP_011539454.1:n.-12+107_-12+109delinsCTG
XM_011541153.1:c.408+107_408+109delinsCTG	XP_011539455.1:n.408+107_408+109delinsCTG
XM_011541154.1:c.408+107_408+109delinsCTG	XP_011539456.1:n.408+107_408+109delinsCTG
XM_011541155.1:c.408+107_408+109delinsCTG	XP_011539457.1:n.408+107_408+109delinsCTG
XM_011541156.1:c.408+107_408+109delinsCTG	XP_011539458.1:n.408+107_408+109delinsCTG
XM_011541157.1:c.-305+107_-305+109delinsCTG	XP_011539459.1:n.-305+107_-305+109delinsCTG
XM_011541154.2:c.408+107_408+109delinsCTG	XP_011539456.1:n.408+107_408+109delinsCTG
NM_012387.3:c.408+107_408+109delinsCTG MANE Select	NP_036519.2:n.408+107_408+109delinsCTG