Canonical Allele Identifier: CA1156200230
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348046A= , CM000663.2:g.17348046A= GRCh38
NC_000001.10:g.17674541A= , CM000663.1:g.17674541A= GRCh37
NC_000001.9:g.17547128A= NCBI36
NG_023261.2:g.44857A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1153A= MANE Select ENSP00000364597.4:p.Met385=
ENST00000468945.1:n.212A=
ENST00000487048.5:n.120A=
NM_012387.2:c.1153A= NP_036519.2:p.Met385=
XM_011541150.1:c.967A= XP_011539452.1:p.Met323=
XM_011541151.1:c.1153A= XP_011539453.1:p.Met385=
XM_011541152.1:c.616A= XP_011539454.1:p.Met206=
XM_011541153.1:c.1153A= XP_011539455.1:p.Met385=
XM_011541154.1:c.1153A= XP_011539456.1:p.Met385=
XM_011541155.1:c.1153A= XP_011539457.1:p.Met385=
XM_011541156.1:c.1153A= XP_011539458.1:p.Met385=
XM_011541157.1:c.262A= XP_011539459.1:p.Met88=
XM_011541154.2:c.1153A= XP_011539456.1:p.Met385=
NM_012387.3:c.1153A= MANE Select NP_036519.2:p.Met385=