Canonical Allele Identifier: CA640743

Gene: PADI4

Linked Data

• dbSNP Id: rs780421882
• ExAC: 1:17672630 TGCAGGTATGTGCCCTGCGGG / T
• gnomAD v2: 1-17672630-TGCAGGTATGTGCCCTGCGGG-T
• gnomAD v3: 1-17346135-TGCAGGTATGTGCCCTGCGGG-T
• gnomAD v4: 1-17346135-TGCAGGTATGTGCCCTGCGGG-T
• MyVariant Identifiers: chr1:g.17672631_17672650del (hg19) ; chr1:g.17346136_17346155del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346141_17346160del , CM000663.2:g.17346141_17346160del	GRCh38
NC_000001.10:g.17672636_17672655del , CM000663.1:g.17672636_17672655del	GRCh37
NC_000001.9:g.17545223_17545242del	NCBI36
NG_023261.2:g.42952_42971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1047+2_1047+21del
ENST00000468945.1:n.106+2_106+21del
NM_012387.2:c.1047+2_1047+21del
XM_011541150.1:c.861+2_861+21del
XM_011541151.1:c.1047+2_1047+21del
XM_011541152.1:c.510+2_510+21del
XM_011541153.1:c.1047+2_1047+21del
XM_011541154.1:c.1047+2_1047+21del
XM_011541155.1:c.1047+2_1047+21del
XM_011541156.1:c.1047+2_1047+21del
XM_011541157.1:c.156+2_156+21del
XM_011541154.2:c.1047+2_1047+21del
NM_012387.3:c.1047+2_1047+21del