Canonical Allele Identifier: CA416411424

Gene: PADI4

Linked Data

• gnomAD v4: 1-17347961-C-T
• MyVariant Identifiers: chr1:g.17674456C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347961C>T , CM000663.2:g.17347961C>T	GRCh38
NC_000001.10:g.17674456C>T , CM000663.1:g.17674456C>T	GRCh37
NC_000001.9:g.17547043C>T	NCBI36
NG_023261.2:g.44772C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1068C>T MANE Select	ENSP00000364597.4:p.Tyr356=
ENST00000468945.1:n.127C>T
ENST00000487048.5:n.35C>T
NM_012387.2:c.1068C>T	NP_036519.2:p.Tyr356=
XM_011541150.1:c.882C>T	XP_011539452.1:p.Tyr294=
XM_011541151.1:c.1068C>T	XP_011539453.1:p.Tyr356=
XM_011541152.1:c.531C>T	XP_011539454.1:p.Tyr177=
XM_011541153.1:c.1068C>T	XP_011539455.1:p.Tyr356=
XM_011541154.1:c.1068C>T	XP_011539456.1:p.Tyr356=
XM_011541155.1:c.1068C>T	XP_011539457.1:p.Tyr356=
XM_011541156.1:c.1068C>T	XP_011539458.1:p.Tyr356=
XM_011541157.1:c.177C>T	XP_011539459.1:p.Tyr59=
XM_011541154.2:c.1068C>T	XP_011539456.1:p.Tyr356=
NM_012387.3:c.1068C>T MANE Select	NP_036519.2:p.Tyr356=