Canonical Allele Identifier: CA1156200639
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348396G= , CM000663.2:g.17348396G= GRCh38
NC_000001.10:g.17674891G= , CM000663.1:g.17674891G= GRCh37
NC_000001.9:g.17547478G= NCBI36
NG_023261.2:g.45207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+348G= MANE Select ENSP00000364597.4:n.1155+348G=
ENST00000487048.5:n.122+348G=
NM_012387.2:c.1155+348G= NP_036519.2:n.1155+348G=
XM_011541150.1:c.969+348G= XP_011539452.1:n.969+348G=
XM_011541151.1:c.1155+348G= XP_011539453.1:n.1155+348G=
XM_011541152.1:c.618+348G= XP_011539454.1:n.618+348G=
XM_011541153.1:c.1156-304G= XP_011539455.1:n.1156-304G=
XM_011541154.1:c.1156-304G= XP_011539456.1:n.1156-304G=
XM_011541155.1:c.1155+348G= XP_011539457.1:n.1155+348G=
XM_011541156.1:c.1155+348G= XP_011539458.1:n.1155+348G=
XM_011541157.1:c.264+348G= XP_011539459.1:n.264+348G=
XM_011541154.2:c.1156-304G= XP_011539456.1:n.1156-304G=
NM_012387.3:c.1155+348G= MANE Select NP_036519.2:n.1155+348G=