Canonical Allele Identifier: CA2643694056

Gene: PADI4

Linked Data

• gnomAD v4: 1-17346158-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346159_17346160del , CM000663.2:g.17346159_17346160del	GRCh38
NC_000001.10:g.17672654_17672655del , CM000663.1:g.17672654_17672655del	GRCh37
NC_000001.9:g.17545241_17545242del	NCBI36
NG_023261.2:g.42970_42971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1047+20_1047+21del MANE Select	ENSP00000364597.4:n.1047+20_1047+21del
ENST00000468945.1:n.106+20_106+21del
NM_012387.2:c.1047+20_1047+21del	NP_036519.2:n.1047+20_1047+21del
XM_011541150.1:c.861+20_861+21del	XP_011539452.1:n.861+20_861+21del
XM_011541151.1:c.1047+20_1047+21del	XP_011539453.1:n.1047+20_1047+21del
XM_011541152.1:c.510+20_510+21del	XP_011539454.1:n.510+20_510+21del
XM_011541153.1:c.1047+20_1047+21del	XP_011539455.1:n.1047+20_1047+21del
XM_011541154.1:c.1047+20_1047+21del	XP_011539456.1:n.1047+20_1047+21del
XM_011541155.1:c.1047+20_1047+21del	XP_011539457.1:n.1047+20_1047+21del
XM_011541156.1:c.1047+20_1047+21del	XP_011539458.1:n.1047+20_1047+21del
XM_011541157.1:c.156+20_156+21del	XP_011539459.1:n.156+20_156+21del
XM_011541154.2:c.1047+20_1047+21del	XP_011539456.1:n.1047+20_1047+21del
NM_012387.3:c.1047+20_1047+21del MANE Select	NP_036519.2:n.1047+20_1047+21del