Canonical Allele Identifier: CA1156184978

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334007_17334008delinsTG , CM000663.2:g.17334007_17334008delinsTG	GRCh38
NC_000001.10:g.17660502_17660503delinsTG , CM000663.1:g.17660502_17660503delinsTG	GRCh37
NC_000001.9:g.17533089_17533090delinsTG	NCBI36
NG_023261.2:g.30818_30819delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.338_339delinsTG MANE Select	ENSP00000364597.4:p.Val113=
ENST00000375453.5:c.338_339delinsTG	ENSP00000364602.1:p.Val113=
NM_012387.2:c.338_339delinsTG	NP_036519.2:p.Val113=
XM_011541150.1:c.338_339delinsTG	XP_011539452.1:p.Val113=
XM_011541151.1:c.338_339delinsTG	XP_011539453.1:p.Val113=
XM_011541152.1:c.-82_-81delinsTG	XP_011539454.1:n.-82_-81delinsTG
XM_011541153.1:c.338_339delinsTG	XP_011539455.1:p.Val113=
XM_011541154.1:c.338_339delinsTG	XP_011539456.1:p.Val113=
XM_011541155.1:c.338_339delinsTG	XP_011539457.1:p.Val113=
XM_011541156.1:c.338_339delinsTG	XP_011539458.1:p.Val113=
XM_011541157.1:c.-375_-374delinsTG	XP_011539459.1:n.-375_-374delinsTG
XM_011541154.2:c.338_339delinsTG	XP_011539456.1:p.Val113=
NM_012387.3:c.338_339delinsTG MANE Select	NP_036519.2:p.Val113=