Canonical Allele Identifier: CA891205083

Gene: PADI4

Linked Data

• dbSNP Id: rs1383147405
• gnomAD v3: 1-17336162-TCTC-T
• gnomAD v4: 1-17336162-TCTC-T
• MyVariant Identifiers: chr1:g.17336163_17336165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336165_17336167del , CM000663.2:g.17336165_17336167del	GRCh38
NC_000001.10:g.17662660_17662662del , CM000663.1:g.17662660_17662662del	GRCh37
NC_000001.9:g.17535247_17535249del	NCBI36
NG_023261.2:g.32976_32978del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.347_349del MANE Select	ENSP00000364597.4:p.Ser116del
NM_012387.2:c.347_349del	NP_036519.2:p.Ser116del
XM_011541150.1:c.340+2156_340+2158del	XP_011539452.1:n.340+2156_340+2158del
XM_011541151.1:c.347_349del	XP_011539453.1:p.Ser116del
XM_011541152.1:c.-73_-71del	XP_011539454.1:n.-73_-71del
XM_011541153.1:c.347_349del	XP_011539455.1:p.Ser116del
XM_011541154.1:c.347_349del	XP_011539456.1:p.Ser116del
XM_011541155.1:c.347_349del	XP_011539457.1:p.Ser116del
XM_011541156.1:c.347_349del	XP_011539458.1:p.Ser116del
XM_011541157.1:c.-366_-364del	XP_011539459.1:n.-366_-364del
XM_011541154.2:c.347_349del	XP_011539456.1:p.Ser116del
NM_012387.3:c.347_349del MANE Select	NP_036519.2:p.Ser116del