Canonical Allele Identifier: CA416403266

Gene: PADI4

Linked Data

• dbSNP Id: rs141897176
• gnomAD v4: 1-17334002-C-A
• MyVariant Identifiers: chr1:g.17660497C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334002C>A , CM000663.2:g.17334002C>A	GRCh38
NC_000001.10:g.17660497C>A , CM000663.1:g.17660497C>A	GRCh37
NC_000001.9:g.17533084C>A	NCBI36
NG_023261.2:g.30813C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.333C>A MANE Select	ENSP00000364597.4:p.Thr111=
ENST00000375453.5:c.333C>A	ENSP00000364602.1:p.Thr111=
NM_012387.2:c.333C>A	NP_036519.2:p.Thr111=
XM_011541150.1:c.333C>A	XP_011539452.1:p.Thr111=
XM_011541151.1:c.333C>A	XP_011539453.1:p.Thr111=
XM_011541152.1:c.-87C>A	XP_011539454.1:n.-87C>A
XM_011541153.1:c.333C>A	XP_011539455.1:p.Thr111=
XM_011541154.1:c.333C>A	XP_011539456.1:p.Thr111=
XM_011541155.1:c.333C>A	XP_011539457.1:p.Thr111=
XM_011541156.1:c.333C>A	XP_011539458.1:p.Thr111=
XM_011541157.1:c.-380C>A	XP_011539459.1:n.-380C>A
XM_011541154.2:c.333C>A	XP_011539456.1:p.Thr111=
NM_012387.3:c.333C>A MANE Select	NP_036519.2:p.Thr111=