Canonical Allele Identifier: CA338236597

Gene: PADI4

Linked Data

• gnomAD v4: 1-17336226-G-T
• MyVariant Identifiers: chr1:g.17662721G>T (hg19) ; chr1:g.17336226G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336226G>T , CM000663.2:g.17336226G>T	GRCh38
NC_000001.10:g.17662721G>T , CM000663.1:g.17662721G>T	GRCh37
NC_000001.9:g.17535308G>T	NCBI36
NG_023261.2:g.33037G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.408G>T MANE Select	ENSP00000364597.4:p.Gln136His
NM_012387.2:c.408G>T	NP_036519.2:p.Gln136His
XM_011541150.1:c.340+2217G>T	XP_011539452.1:n.340+2217G>T
XM_011541151.1:c.408G>T	XP_011539453.1:p.Gln136His
XM_011541152.1:c.-12G>T	XP_011539454.1:n.-12G>T
XM_011541153.1:c.408G>T	XP_011539455.1:p.Gln136His
XM_011541154.1:c.408G>T	XP_011539456.1:p.Gln136His
XM_011541155.1:c.408G>T	XP_011539457.1:p.Gln136His
XM_011541156.1:c.408G>T	XP_011539458.1:p.Gln136His
XM_011541157.1:c.-305G>T	XP_011539459.1:n.-305G>T
XM_011541154.2:c.408G>T	XP_011539456.1:p.Gln136His
NM_012387.3:c.408G>T MANE Select	NP_036519.2:p.Gln136His