Canonical Allele Identifier: CA338248419

Gene: PADI4

Linked Data

• gnomAD v4: 1-17346140-G-A
• MyVariant Identifiers: chr1:g.17672635G>A (hg19) ; chr1:g.17346140G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346140G>A , CM000663.2:g.17346140G>A	GRCh38
NC_000001.10:g.17672635G>A , CM000663.1:g.17672635G>A	GRCh37
NC_000001.9:g.17545222G>A	NCBI36
NG_023261.2:g.42951G>A

Transcript Alleles

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