Canonical Allele Identifier: CA521042338

Gene: PADI4

Linked Data

• dbSNP Id: rs1220064442
• gnomAD v2: 1-17660801-A-ATT
• gnomAD v4: 1-17334306-A-ATT
• MyVariant Identifiers: chr1:g.17660801_17660802insTT (hg19) ; chr1:g.17334306_17334307insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334306_17334307insTT , CM000663.2:g.17334306_17334307insTT	GRCh38
NC_000001.10:g.17660801_17660802insTT , CM000663.1:g.17660801_17660802insTT	GRCh37
NC_000001.9:g.17533388_17533389insTT	NCBI36
NG_023261.2:g.31117_31118insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+297_340+298insTT MANE Select	ENSP00000364597.4:n.340+297_340+298insTT
ENST00000375453.5:c.341-18_341-17insTT	ENSP00000364602.1:n.341-18_341-17insTT
NM_012387.2:c.340+297_340+298insTT	NP_036519.2:n.340+297_340+298insTT
XM_011541150.1:c.340+297_340+298insTT	XP_011539452.1:n.340+297_340+298insTT
XM_011541151.1:c.340+297_340+298insTT	XP_011539453.1:n.340+297_340+298insTT
XM_011541152.1:c.-80+297_-80+298insTT	XP_011539454.1:n.-80+297_-80+298insTT
XM_011541153.1:c.340+297_340+298insTT	XP_011539455.1:n.340+297_340+298insTT
XM_011541154.1:c.340+297_340+298insTT	XP_011539456.1:n.340+297_340+298insTT
XM_011541155.1:c.340+297_340+298insTT	XP_011539457.1:n.340+297_340+298insTT
XM_011541156.1:c.340+297_340+298insTT	XP_011539458.1:n.340+297_340+298insTT
XM_011541157.1:c.-373+297_-373+298insTT	XP_011539459.1:n.-373+297_-373+298insTT
XM_011541154.2:c.340+297_340+298insTT	XP_011539456.1:n.340+297_340+298insTT
NM_012387.3:c.340+297_340+298insTT MANE Select	NP_036519.2:n.340+297_340+298insTT