Canonical Allele Identifier: CA2643694173

Gene: PADI4

Linked Data

• gnomAD v4: 1-17346251-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346251A>G , CM000663.2:g.17346251A>G	GRCh38
NC_000001.10:g.17672746A>G , CM000663.1:g.17672746A>G	GRCh37
NC_000001.9:g.17545333A>G	NCBI36
NG_023261.2:g.43062A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.1047+112A>G MANE Select	ENSP00000364597.4:n.1047+112A>G
ENST00000468945.1:n.106+112A>G
NM_012387.2:c.1047+112A>G	NP_036519.2:n.1047+112A>G
XM_011541150.1:c.861+112A>G	XP_011539452.1:n.861+112A>G
XM_011541151.1:c.1047+112A>G	XP_011539453.1:n.1047+112A>G
XM_011541152.1:c.510+112A>G	XP_011539454.1:n.510+112A>G
XM_011541153.1:c.1047+112A>G	XP_011539455.1:n.1047+112A>G
XM_011541154.1:c.1047+112A>G	XP_011539456.1:n.1047+112A>G
XM_011541155.1:c.1047+112A>G	XP_011539457.1:n.1047+112A>G
XM_011541156.1:c.1047+112A>G	XP_011539458.1:n.1047+112A>G
XM_011541157.1:c.156+112A>G	XP_011539459.1:n.156+112A>G
XM_011541154.2:c.1047+112A>G	XP_011539456.1:n.1047+112A>G
NM_012387.3:c.1047+112A>G MANE Select	NP_036519.2:n.1047+112A>G