Canonical Allele Identifier: CA2643694473

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348147-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348148_17348149del , CM000663.2:g.17348148_17348149del	GRCh38
NC_000001.10:g.17674643_17674644del , CM000663.1:g.17674643_17674644del	GRCh37
NC_000001.9:g.17547230_17547231del	NCBI36
NG_023261.2:g.44959_44960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+100_1155+101del MANE Select	ENSP00000364597.4:n.1155+100_1155+101del
ENST00000468945.1:n.314_315del
ENST00000487048.5:n.122+100_122+101del
NM_012387.2:c.1155+100_1155+101del	NP_036519.2:n.1155+100_1155+101del
XM_011541150.1:c.969+100_969+101del	XP_011539452.1:n.969+100_969+101del
XM_011541151.1:c.1155+100_1155+101del	XP_011539453.1:n.1155+100_1155+101del
XM_011541152.1:c.618+100_618+101del	XP_011539454.1:n.618+100_618+101del
XM_011541153.1:c.1155+100_1155+101del	XP_011539455.1:n.1155+100_1155+101del
XM_011541154.1:c.1155+100_1155+101del	XP_011539456.1:n.1155+100_1155+101del
XM_011541155.1:c.1155+100_1155+101del	XP_011539457.1:n.1155+100_1155+101del
XM_011541156.1:c.1155+100_1155+101del	XP_011539458.1:n.1155+100_1155+101del
XM_011541157.1:c.264+100_264+101del	XP_011539459.1:n.264+100_264+101del
XM_011541154.2:c.1155+100_1155+101del	XP_011539456.1:n.1155+100_1155+101del
NM_012387.3:c.1155+100_1155+101del MANE Select	NP_036519.2:n.1155+100_1155+101del