Canonical Allele Identifier: CA2742645105

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348424_17348425insA , CM000663.2:g.17348424_17348425insA	GRCh38
NC_000001.10:g.17674919_17674920insA , CM000663.1:g.17674919_17674920insA	GRCh37
NC_000001.9:g.17547506_17547507insA	NCBI36
NG_023261.2:g.45235_45236insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+376_1155+377insA MANE Select	ENSP00000364597.4:n.1155+376_1155+377insA
ENST00000487048.5:n.122+376_122+377insA
NM_012387.2:c.1155+376_1155+377insA	NP_036519.2:n.1155+376_1155+377insA
XM_011541150.1:c.969+376_969+377insA	XP_011539452.1:n.969+376_969+377insA
XM_011541151.1:c.1155+376_1155+377insA	XP_011539453.1:n.1155+376_1155+377insA
XM_011541152.1:c.618+376_618+377insA	XP_011539454.1:n.618+376_618+377insA
XM_011541153.1:c.1156-276_1156-275insA	XP_011539455.1:n.1156-276_1156-275insA
XM_011541154.1:c.1156-276_1156-275insA	XP_011539456.1:n.1156-276_1156-275insA
XM_011541155.1:c.1155+376_1155+377insA	XP_011539457.1:n.1155+376_1155+377insA
XM_011541156.1:c.1155+376_1155+377insA	XP_011539458.1:n.1155+376_1155+377insA
XM_011541157.1:c.264+376_264+377insA	XP_011539459.1:n.264+376_264+377insA
XM_011541154.2:c.1156-276_1156-275insA	XP_011539456.1:n.1156-276_1156-275insA
NM_012387.3:c.1155+376_1155+377insA MANE Select	NP_036519.2:n.1155+376_1155+377insA