Canonical Allele Identifier: CA640412

Gene: PADI4

Linked Data

• dbSNP Id: rs575630557
• ExAC: 1:17660495 A / T
• gnomAD v2: 1-17660495-A-T
• gnomAD v4: 1-17334000-A-T
• MyVariant Identifiers: chr1:g.17660495A>T (hg19) ; chr1:g.17334000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334000A>T , CM000663.2:g.17334000A>T	GRCh38
NC_000001.10:g.17660495A>T , CM000663.1:g.17660495A>T	GRCh37
NC_000001.9:g.17533082A>T	NCBI36
NG_023261.2:g.30811A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.331A>T MANE Select	ENSP00000364597.4:p.Thr111Ser
ENST00000375453.5:c.331A>T	ENSP00000364602.1:p.Thr111Ser
NM_012387.2:c.331A>T	NP_036519.2:p.Thr111Ser
XM_011541150.1:c.331A>T	XP_011539452.1:p.Thr111Ser
XM_011541151.1:c.331A>T	XP_011539453.1:p.Thr111Ser
XM_011541152.1:c.-89A>T	XP_011539454.1:n.-89A>T
XM_011541153.1:c.331A>T	XP_011539455.1:p.Thr111Ser
XM_011541154.1:c.331A>T	XP_011539456.1:p.Thr111Ser
XM_011541155.1:c.331A>T	XP_011539457.1:p.Thr111Ser
XM_011541156.1:c.331A>T	XP_011539458.1:p.Thr111Ser
XM_011541157.1:c.-382A>T	XP_011539459.1:n.-382A>T
XM_011541154.2:c.331A>T	XP_011539456.1:p.Thr111Ser
NM_012387.3:c.331A>T MANE Select	NP_036519.2:p.Thr111Ser