Canonical Allele Identifier: CA640774

Gene: PADI4

Linked Data

• dbSNP Id: rs566560922
• ExAC: 1:17674474 A / G
• gnomAD v3: 1-17347979-A-G
• gnomAD v4: 1-17347979-A-G
• MyVariant Identifiers: chr1:g.17674474A>G (hg19) ; chr1:g.17347979A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347979A>G , CM000663.2:g.17347979A>G	GRCh38
NC_000001.10:g.17674474A>G , CM000663.1:g.17674474A>G	GRCh37
NC_000001.9:g.17547061A>G	NCBI36
NG_023261.2:g.44790A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1086A>G MANE Select	ENSP00000364597.4:p.Lys362=
ENST00000468945.1:n.145A>G
ENST00000487048.5:n.53A>G
NM_012387.2:c.1086A>G	NP_036519.2:p.Lys362=
XM_011541150.1:c.900A>G	XP_011539452.1:p.Lys300=
XM_011541151.1:c.1086A>G	XP_011539453.1:p.Lys362=
XM_011541152.1:c.549A>G	XP_011539454.1:p.Lys183=
XM_011541153.1:c.1086A>G	XP_011539455.1:p.Lys362=
XM_011541154.1:c.1086A>G	XP_011539456.1:p.Lys362=
XM_011541155.1:c.1086A>G	XP_011539457.1:p.Lys362=
XM_011541156.1:c.1086A>G	XP_011539458.1:p.Lys362=
XM_011541157.1:c.195A>G	XP_011539459.1:p.Lys65=
XM_011541154.2:c.1086A>G	XP_011539456.1:p.Lys362=
NM_012387.3:c.1086A>G MANE Select	NP_036519.2:p.Lys362=