Canonical Allele Identifier: CA416404766

Gene: PADI4

Linked Data

• gnomAD v4: 1-17336166-C-T
• MyVariant Identifiers: chr1:g.17662661C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336166C>T , CM000663.2:g.17336166C>T	GRCh38
NC_000001.10:g.17662661C>T , CM000663.1:g.17662661C>T	GRCh37
NC_000001.9:g.17535248C>T	NCBI36
NG_023261.2:g.32977C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.348C>T MANE Select	ENSP00000364597.4:p.Ser116=
NM_012387.2:c.348C>T	NP_036519.2:p.Ser116=
XM_011541150.1:c.340+2157C>T	XP_011539452.1:n.340+2157C>T
XM_011541151.1:c.348C>T	XP_011539453.1:p.Ser116=
XM_011541152.1:c.-72C>T	XP_011539454.1:n.-72C>T
XM_011541153.1:c.348C>T	XP_011539455.1:p.Ser116=
XM_011541154.1:c.348C>T	XP_011539456.1:p.Ser116=
XM_011541155.1:c.348C>T	XP_011539457.1:p.Ser116=
XM_011541156.1:c.348C>T	XP_011539458.1:p.Ser116=
XM_011541157.1:c.-365C>T	XP_011539459.1:n.-365C>T
XM_011541154.2:c.348C>T	XP_011539456.1:p.Ser116=
NM_012387.3:c.348C>T MANE Select	NP_036519.2:p.Ser116=