Canonical Allele Identifier: CA416411517

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17674465C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347970C>G , CM000663.2:g.17347970C>G	GRCh38
NC_000001.10:g.17674465C>G , CM000663.1:g.17674465C>G	GRCh37
NC_000001.9:g.17547052C>G	NCBI36
NG_023261.2:g.44781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1077C>G MANE Select	ENSP00000364597.4:p.Ala359=
ENST00000468945.1:n.136C>G
ENST00000487048.5:n.44C>G
NM_012387.2:c.1077C>G	NP_036519.2:p.Ala359=
XM_011541150.1:c.891C>G	XP_011539452.1:p.Ala297=
XM_011541151.1:c.1077C>G	XP_011539453.1:p.Ala359=
XM_011541152.1:c.540C>G	XP_011539454.1:p.Ala180=
XM_011541153.1:c.1077C>G	XP_011539455.1:p.Ala359=
XM_011541154.1:c.1077C>G	XP_011539456.1:p.Ala359=
XM_011541155.1:c.1077C>G	XP_011539457.1:p.Ala359=
XM_011541156.1:c.1077C>G	XP_011539458.1:p.Ala359=
XM_011541157.1:c.186C>G	XP_011539459.1:p.Ala62=
XM_011541154.2:c.1077C>G	XP_011539456.1:p.Ala359=
NM_012387.3:c.1077C>G MANE Select	NP_036519.2:p.Ala359=