Canonical Allele Identifier: CA18633771

Gene: PADI4

Linked Data

• dbSNP Id: rs6698443
• MyVariant Identifiers: chr1:g.17332069C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17332069C>A , CM000663.2:g.17332069C>A	GRCh38
NC_000001.10:g.17658564C>A , CM000663.1:g.17658564C>A	GRCh37
NC_000001.9:g.17531151C>A	NCBI36
NG_023261.2:g.28880C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.273+920C>A MANE Select	ENSP00000364597.4:n.273+920C>A
ENST00000375453.5:c.273+920C>A	ENSP00000364602.1:n.273+920C>A
NM_012387.2:c.273+920C>A	NP_036519.2:n.273+920C>A
XM_011541150.1:c.273+920C>A	XP_011539452.1:n.273+920C>A
XM_011541151.1:c.273+920C>A	XP_011539453.1:n.273+920C>A
XM_011541153.1:c.273+920C>A	XP_011539455.1:n.273+920C>A
XM_011541154.1:c.273+920C>A	XP_011539456.1:n.273+920C>A
XM_011541155.1:c.273+920C>A	XP_011539457.1:n.273+920C>A
XM_011541156.1:c.273+920C>A	XP_011539458.1:n.273+920C>A
XM_011541154.2:c.273+920C>A	XP_011539456.1:n.273+920C>A
NM_012387.3:c.273+920C>A MANE Select	NP_036519.2:n.273+920C>A