Canonical Allele Identifier: CA1143944857
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336261A= , CM000663.2:g.17336261A= GRCh38
NC_000001.10:g.17662756A= , CM000663.1:g.17662756A= GRCh37
NC_000001.9:g.17535343A= NCBI36
NG_023261.2:g.33072A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.408+35A= MANE Select ENSP00000364597.4:n.408+35A=
NM_012387.2:c.408+35A= NP_036519.2:n.408+35A=
XM_011541150.1:c.340+2252A= XP_011539452.1:n.340+2252A=
XM_011541151.1:c.408+35A= XP_011539453.1:n.408+35A=
XM_011541152.1:c.-12+35A= XP_011539454.1:n.-12+35A=
XM_011541153.1:c.408+35A= XP_011539455.1:n.408+35A=
XM_011541154.1:c.408+35A= XP_011539456.1:n.408+35A=
XM_011541155.1:c.408+35A= XP_011539457.1:n.408+35A=
XM_011541156.1:c.408+35A= XP_011539458.1:n.408+35A=
XM_011541157.1:c.-305+35A= XP_011539459.1:n.-305+35A=
XM_011541154.2:c.408+35A= XP_011539456.1:n.408+35A=
NM_012387.3:c.408+35A= MANE Select NP_036519.2:n.408+35A=