Canonical Allele Identifier: CA2643698572
Gene: PADI4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17334307_17334308insATT , CM000663.2:g.17334307_17334308insATT GRCh38
NC_000001.10:g.17660802_17660803insATT , CM000663.1:g.17660802_17660803insATT GRCh37
NC_000001.9:g.17533389_17533390insATT NCBI36
NG_023261.2:g.31118_31119insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.340+298_340+299insATT MANE Select ENSP00000364597.4:n.340+298_340+299insATT
ENST00000375453.5:c.341-17_341-16insATT ENSP00000364602.1:n.341-17_341-16insATT
NM_012387.2:c.340+298_340+299insATT NP_036519.2:n.340+298_340+299insATT
XM_011541150.1:c.340+298_340+299insATT XP_011539452.1:n.340+298_340+299insATT
XM_011541151.1:c.340+298_340+299insATT XP_011539453.1:n.340+298_340+299insATT
XM_011541152.1:c.-80+298_-80+299insATT XP_011539454.1:n.-80+298_-80+299insATT
XM_011541153.1:c.340+298_340+299insATT XP_011539455.1:n.340+298_340+299insATT
XM_011541154.1:c.340+298_340+299insATT XP_011539456.1:n.340+298_340+299insATT
XM_011541155.1:c.340+298_340+299insATT XP_011539457.1:n.340+298_340+299insATT
XM_011541156.1:c.340+298_340+299insATT XP_011539458.1:n.340+298_340+299insATT
XM_011541157.1:c.-373+298_-373+299insATT XP_011539459.1:n.-373+298_-373+299insATT
XM_011541154.2:c.340+298_340+299insATT XP_011539456.1:n.340+298_340+299insATT
NM_012387.3:c.340+298_340+299insATT MANE Select NP_036519.2:n.340+298_340+299insATT