Canonical Allele Identifier: CA338256238

Gene: PADI4

Linked Data

• gnomAD v4: 1-17356029-G-A
• MyVariant Identifiers: chr1:g.17682524G>A (hg19) ; chr1:g.17356029G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17356029G>A , CM000663.2:g.17356029G>A	GRCh38
NC_000001.10:g.17682524G>A , CM000663.1:g.17682524G>A	GRCh37
NC_000001.9:g.17555111G>A	NCBI36
NG_023261.2:g.52840G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1357G>A MANE Select	ENSP00000364597.4:p.Ala453Thr
ENST00000467001.1:n.258G>A
ENST00000487048.5:n.324G>A
NM_012387.2:c.1357G>A	NP_036519.2:p.Ala453Thr
XM_011541150.1:c.1171G>A	XP_011539452.1:p.Ala391Thr
XM_011541151.1:c.1156-328G>A	XP_011539453.1:n.1156-328G>A
XM_011541152.1:c.820G>A	XP_011539454.1:p.Ala274Thr
XM_011541154.1:c.*94G>A	XP_011539456.1:n.*94G>A
XM_011541156.1:c.*41G>A	XP_011539458.1:n.*41G>A
XM_011541157.1:c.466G>A	XP_011539459.1:p.Ala156Thr
XM_011541154.2:c.*94G>A	XP_011539456.1:n.*94G>A
NM_012387.3:c.1357G>A MANE Select	NP_036519.2:p.Ala453Thr