Canonical Allele Identifier: CA416412232

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348045-G-A
• MyVariant Identifiers: chr1:g.17674540G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348045G>A , CM000663.2:g.17348045G>A	GRCh38
NC_000001.10:g.17674540G>A , CM000663.1:g.17674540G>A	GRCh37
NC_000001.9:g.17547127G>A	NCBI36
NG_023261.2:g.44856G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1152G>A MANE Select	ENSP00000364597.4:p.Val384=
ENST00000468945.1:n.211G>A
ENST00000487048.5:n.119G>A
NM_012387.2:c.1152G>A	NP_036519.2:p.Val384=
XM_011541150.1:c.966G>A	XP_011539452.1:p.Val322=
XM_011541151.1:c.1152G>A	XP_011539453.1:p.Val384=
XM_011541152.1:c.615G>A	XP_011539454.1:p.Val205=
XM_011541153.1:c.1152G>A	XP_011539455.1:p.Val384=
XM_011541154.1:c.1152G>A	XP_011539456.1:p.Val384=
XM_011541155.1:c.1152G>A	XP_011539457.1:p.Val384=
XM_011541156.1:c.1152G>A	XP_011539458.1:p.Val384=
XM_011541157.1:c.261G>A	XP_011539459.1:p.Val87=
XM_011541154.2:c.1152G>A	XP_011539456.1:p.Val384=
NM_012387.3:c.1152G>A MANE Select	NP_036519.2:p.Val384=