Canonical Allele Identifier: CA416411920

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17674507C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348012C>T , CM000663.2:g.17348012C>T	GRCh38
NC_000001.10:g.17674507C>T , CM000663.1:g.17674507C>T	GRCh37
NC_000001.9:g.17547094C>T	NCBI36
NG_023261.2:g.44823C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1119C>T MANE Select	ENSP00000364597.4:p.Asn373=
ENST00000468945.1:n.178C>T
ENST00000487048.5:n.86C>T
NM_012387.2:c.1119C>T	NP_036519.2:p.Asn373=
XM_011541150.1:c.933C>T	XP_011539452.1:p.Asn311=
XM_011541151.1:c.1119C>T	XP_011539453.1:p.Asn373=
XM_011541152.1:c.582C>T	XP_011539454.1:p.Asn194=
XM_011541153.1:c.1119C>T	XP_011539455.1:p.Asn373=
XM_011541154.1:c.1119C>T	XP_011539456.1:p.Asn373=
XM_011541155.1:c.1119C>T	XP_011539457.1:p.Asn373=
XM_011541156.1:c.1119C>T	XP_011539458.1:p.Asn373=
XM_011541157.1:c.228C>T	XP_011539459.1:p.Asn76=
XM_011541154.2:c.1119C>T	XP_011539456.1:p.Asn373=
NM_012387.3:c.1119C>T MANE Select	NP_036519.2:p.Asn373=