Canonical Allele Identifier: CA640487

Gene: PADI4

Linked Data

• dbSNP Id: rs371817002
• ExAC: 1:17662706 A / G
• gnomAD v2: 1-17662706-A-G
• gnomAD v3: 1-17336211-A-G
• gnomAD v4: 1-17336211-A-G
• MyVariant Identifiers: chr1:g.17662706A>G (hg19) ; chr1:g.17336211A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336211A>G , CM000663.2:g.17336211A>G	GRCh38
NC_000001.10:g.17662706A>G , CM000663.1:g.17662706A>G	GRCh37
NC_000001.9:g.17535293A>G	NCBI36
NG_023261.2:g.33022A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.393A>G MANE Select	ENSP00000364597.4:p.Arg131=
NM_012387.2:c.393A>G	NP_036519.2:p.Arg131=
XM_011541150.1:c.340+2202A>G	XP_011539452.1:n.340+2202A>G
XM_011541151.1:c.393A>G	XP_011539453.1:p.Arg131=
XM_011541152.1:c.-27A>G	XP_011539454.1:n.-27A>G
XM_011541153.1:c.393A>G	XP_011539455.1:p.Arg131=
XM_011541154.1:c.393A>G	XP_011539456.1:p.Arg131=
XM_011541155.1:c.393A>G	XP_011539457.1:p.Arg131=
XM_011541156.1:c.393A>G	XP_011539458.1:p.Arg131=
XM_011541157.1:c.-320A>G	XP_011539459.1:n.-320A>G
XM_011541154.2:c.393A>G	XP_011539456.1:p.Arg131=
NM_012387.3:c.393A>G MANE Select	NP_036519.2:p.Arg131=