Canonical Allele Identifier: CA338236435

Gene: PADI4

Linked Data

• gnomAD v4: 1-17336203-C-A
• MyVariant Identifiers: chr1:g.17662698C>A (hg19) ; chr1:g.17336203C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336203C>A , CM000663.2:g.17336203C>A	GRCh38
NC_000001.10:g.17662698C>A , CM000663.1:g.17662698C>A	GRCh37
NC_000001.9:g.17535285C>A	NCBI36
NG_023261.2:g.33014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.385C>A MANE Select	ENSP00000364597.4:p.Pro129Thr
NM_012387.2:c.385C>A	NP_036519.2:p.Pro129Thr
XM_011541150.1:c.340+2194C>A	XP_011539452.1:n.340+2194C>A
XM_011541151.1:c.385C>A	XP_011539453.1:p.Pro129Thr
XM_011541152.1:c.-35C>A	XP_011539454.1:n.-35C>A
XM_011541153.1:c.385C>A	XP_011539455.1:p.Pro129Thr
XM_011541154.1:c.385C>A	XP_011539456.1:p.Pro129Thr
XM_011541155.1:c.385C>A	XP_011539457.1:p.Pro129Thr
XM_011541156.1:c.385C>A	XP_011539458.1:p.Pro129Thr
XM_011541157.1:c.-328C>A	XP_011539459.1:n.-328C>A
XM_011541154.2:c.385C>A	XP_011539456.1:p.Pro129Thr
NM_012387.3:c.385C>A MANE Select	NP_036519.2:p.Pro129Thr