Canonical Allele Identifier: CA2643698564
Gene: PADI4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334306_17334307insTTT , CM000663.2:g.17334306_17334307insTTT GRCh38
NC_000001.10:g.17660801_17660802insTTT , CM000663.1:g.17660801_17660802insTTT GRCh37
NC_000001.9:g.17533388_17533389insTTT NCBI36
NG_023261.2:g.31117_31118insTTT

Transcript Alleles

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