Canonical Allele Identifier: CA891204267
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs1193166377
MyVariant Identifiers: chr1:g.17334008del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334010del , CM000663.2:g.17334010del GRCh38
NC_000001.10:g.17660505del , CM000663.1:g.17660505del GRCh37
NC_000001.9:g.17533092del NCBI36
NG_023261.2:g.30821del

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.340+1del
ENST00000375453.5:c.340+1del
NM_012387.2:c.340+1del
XM_011541150.1:c.340+1del
XM_011541151.1:c.340+1del
XM_011541152.1:c.-80+1del
XM_011541153.1:c.340+1del
XM_011541154.1:c.340+1del
XM_011541155.1:c.340+1del
XM_011541156.1:c.340+1del
XM_011541157.1:c.-373+1del
XM_011541154.2:c.340+1del
NM_012387.3:c.340+1del