Canonical Allele Identifier: CA1156236355

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17332009_17332010delinsAG , CM000663.2:g.17332009_17332010delinsAG	GRCh38
NC_000001.10:g.17658504_17658505delinsAG , CM000663.1:g.17658504_17658505delinsAG	GRCh37
NC_000001.9:g.17531091_17531092delinsAG	NCBI36
NG_023261.2:g.28820_28821delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.273+860_273+861delinsAG MANE Select	ENSP00000364597.4:n.273+860_273+861delinsAG
ENST00000375453.5:c.273+860_273+861delinsAG	ENSP00000364602.1:n.273+860_273+861delinsAG
NM_012387.2:c.273+860_273+861delinsAG	NP_036519.2:n.273+860_273+861delinsAG
XM_011541150.1:c.273+860_273+861delinsAG	XP_011539452.1:n.273+860_273+861delinsAG
XM_011541151.1:c.273+860_273+861delinsAG	XP_011539453.1:n.273+860_273+861delinsAG
XM_011541153.1:c.273+860_273+861delinsAG	XP_011539455.1:n.273+860_273+861delinsAG
XM_011541154.1:c.273+860_273+861delinsAG	XP_011539456.1:n.273+860_273+861delinsAG
XM_011541155.1:c.273+860_273+861delinsAG	XP_011539457.1:n.273+860_273+861delinsAG
XM_011541156.1:c.273+860_273+861delinsAG	XP_011539458.1:n.273+860_273+861delinsAG
XM_011541154.2:c.273+860_273+861delinsAG	XP_011539456.1:n.273+860_273+861delinsAG
NM_012387.3:c.273+860_273+861delinsAG MANE Select	NP_036519.2:n.273+860_273+861delinsAG