Canonical Allele Identifier: CA416411398

Gene: PADI4

Linked Data

• dbSNP Id: rs1275080963
• gnomAD v3: 1-17347958-C-T
• gnomAD v4: 1-17347958-C-T
• MyVariant Identifiers: chr1:g.17674453C>T (hg19) ; chr1:g.17347958C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347958C>T , CM000663.2:g.17347958C>T	GRCh38
NC_000001.10:g.17674453C>T , CM000663.1:g.17674453C>T	GRCh37
NC_000001.9:g.17547040C>T	NCBI36
NG_023261.2:g.44769C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1065C>T MANE Select	ENSP00000364597.4:p.Gly355=
ENST00000468945.1:n.124C>T
ENST00000487048.5:n.32C>T
NM_012387.2:c.1065C>T	NP_036519.2:p.Gly355=
XM_011541150.1:c.879C>T	XP_011539452.1:p.Gly293=
XM_011541151.1:c.1065C>T	XP_011539453.1:p.Gly355=
XM_011541152.1:c.528C>T	XP_011539454.1:p.Gly176=
XM_011541153.1:c.1065C>T	XP_011539455.1:p.Gly355=
XM_011541154.1:c.1065C>T	XP_011539456.1:p.Gly355=
XM_011541155.1:c.1065C>T	XP_011539457.1:p.Gly355=
XM_011541156.1:c.1065C>T	XP_011539458.1:p.Gly355=
XM_011541157.1:c.174C>T	XP_011539459.1:p.Gly58=
XM_011541154.2:c.1065C>T	XP_011539456.1:p.Gly355=
NM_012387.3:c.1065C>T MANE Select	NP_036519.2:p.Gly355=