Canonical Allele Identifier: CA640496

Gene: PADI4

Linked Data

• dbSNP Id: rs775181456
• ExAC: 1:17662742 C / A
• gnomAD v4: 1-17336247-C-A
• MyVariant Identifiers: chr1:g.17662742C>A (hg19) ; chr1:g.17336247C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336247C>A , CM000663.2:g.17336247C>A	GRCh38
NC_000001.10:g.17662742C>A , CM000663.1:g.17662742C>A	GRCh37
NC_000001.9:g.17535329C>A	NCBI36
NG_023261.2:g.33058C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.408+21C>A MANE Select	ENSP00000364597.4:n.408+21C>A
NM_012387.2:c.408+21C>A	NP_036519.2:n.408+21C>A
XM_011541150.1:c.340+2238C>A	XP_011539452.1:n.340+2238C>A
XM_011541151.1:c.408+21C>A	XP_011539453.1:n.408+21C>A
XM_011541152.1:c.-12+21C>A	XP_011539454.1:n.-12+21C>A
XM_011541153.1:c.408+21C>A	XP_011539455.1:n.408+21C>A
XM_011541154.1:c.408+21C>A	XP_011539456.1:n.408+21C>A
XM_011541155.1:c.408+21C>A	XP_011539457.1:n.408+21C>A
XM_011541156.1:c.408+21C>A	XP_011539458.1:n.408+21C>A
XM_011541157.1:c.-305+21C>A	XP_011539459.1:n.-305+21C>A
XM_011541154.2:c.408+21C>A	XP_011539456.1:n.408+21C>A
NM_012387.3:c.408+21C>A MANE Select	NP_036519.2:n.408+21C>A