Canonical Allele Identifier: CA1156200495
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348271C= , CM000663.2:g.17348271C= GRCh38
NC_000001.10:g.17674766C= , CM000663.1:g.17674766C= GRCh37
NC_000001.9:g.17547353C= NCBI36
NG_023261.2:g.45082C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+223C= MANE Select ENSP00000364597.4:n.1155+223C=
ENST00000487048.5:n.122+223C=
NM_012387.2:c.1155+223C= NP_036519.2:n.1155+223C=
XM_011541150.1:c.969+223C= XP_011539452.1:n.969+223C=
XM_011541151.1:c.1155+223C= XP_011539453.1:n.1155+223C=
XM_011541152.1:c.618+223C= XP_011539454.1:n.618+223C=
XM_011541153.1:c.1155+223C= XP_011539455.1:n.1155+223C=
XM_011541154.1:c.1155+223C= XP_011539456.1:n.1155+223C=
XM_011541155.1:c.1155+223C= XP_011539457.1:n.1155+223C=
XM_011541156.1:c.1155+223C= XP_011539458.1:n.1155+223C=
XM_011541157.1:c.264+223C= XP_011539459.1:n.264+223C=
XM_011541154.2:c.1155+223C= XP_011539456.1:n.1155+223C=
NM_012387.3:c.1155+223C= MANE Select NP_036519.2:n.1155+223C=