Canonical Allele Identifier: CA891210588

Gene: PADI4

Linked Data

• dbSNP Id: rs1403137863
• gnomAD v3: 1-17346152-CG-C
• gnomAD v4: 1-17346152-CG-C
• MyVariant Identifiers: chr1:g.17346153del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346156del , CM000663.2:g.17346156del	GRCh38
NC_000001.10:g.17672651del , CM000663.1:g.17672651del	GRCh37
NC_000001.9:g.17545238del	NCBI36
NG_023261.2:g.42967del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.1047+17del MANE Select	ENSP00000364597.4:n.1047+17del
ENST00000468945.1:n.106+17del
NM_012387.2:c.1047+17del	NP_036519.2:n.1047+17del
XM_011541150.1:c.861+17del	XP_011539452.1:n.861+17del
XM_011541151.1:c.1047+17del	XP_011539453.1:n.1047+17del
XM_011541152.1:c.510+17del	XP_011539454.1:n.510+17del
XM_011541153.1:c.1047+17del	XP_011539455.1:n.1047+17del
XM_011541154.1:c.1047+17del	XP_011539456.1:n.1047+17del
XM_011541155.1:c.1047+17del	XP_011539457.1:n.1047+17del
XM_011541156.1:c.1047+17del	XP_011539458.1:n.1047+17del
XM_011541157.1:c.156+17del	XP_011539459.1:n.156+17del
XM_011541154.2:c.1047+17del	XP_011539456.1:n.1047+17del
NM_012387.3:c.1047+17del MANE Select	NP_036519.2:n.1047+17del