Canonical Allele Identifier: CA916119034
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs34965359

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334310_17334320dup , CM000663.2:g.17334310_17334320dup GRCh38
NC_000001.10:g.17660805_17660815dup , CM000663.1:g.17660805_17660815dup GRCh37
NC_000001.9:g.17533392_17533402dup NCBI36
NG_023261.2:g.31121_31131dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.340+301_340+311dup MANE Select ENSP00000364597.4:n.340+301_340+311dup
ENST00000375453.5:c.341-14_341-4dup ENSP00000364602.1:n.341-14_341-4dup
NM_012387.2:c.340+301_340+311dup NP_036519.2:n.340+301_340+311dup
XM_011541150.1:c.340+301_340+311dup XP_011539452.1:n.340+301_340+311dup
XM_011541151.1:c.340+301_340+311dup XP_011539453.1:n.340+301_340+311dup
XM_011541152.1:c.-80+301_-80+311dup XP_011539454.1:n.-80+301_-80+311dup
XM_011541153.1:c.340+301_340+311dup XP_011539455.1:n.340+301_340+311dup
XM_011541154.1:c.340+301_340+311dup XP_011539456.1:n.340+301_340+311dup
XM_011541155.1:c.340+301_340+311dup XP_011539457.1:n.340+301_340+311dup
XM_011541156.1:c.340+301_340+311dup XP_011539458.1:n.340+301_340+311dup
XM_011541157.1:c.-373+301_-373+311dup XP_011539459.1:n.-373+301_-373+311dup
XM_011541154.2:c.340+301_340+311dup XP_011539456.1:n.340+301_340+311dup
NM_012387.3:c.340+301_340+311dup MANE Select NP_036519.2:n.340+301_340+311dup