Canonical Allele Identifier: CA1156198067
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17346236G= , CM000663.2:g.17346236G= GRCh38
NC_000001.10:g.17672731G= , CM000663.1:g.17672731G= GRCh37
NC_000001.9:g.17545318G= NCBI36
NG_023261.2:g.43047G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.1047+97G= MANE Select ENSP00000364597.4:n.1047+97G=
ENST00000468945.1:n.106+97G=
NM_012387.2:c.1047+97G= NP_036519.2:n.1047+97G=
XM_011541150.1:c.861+97G= XP_011539452.1:n.861+97G=
XM_011541151.1:c.1047+97G= XP_011539453.1:n.1047+97G=
XM_011541152.1:c.510+97G= XP_011539454.1:n.510+97G=
XM_011541153.1:c.1047+97G= XP_011539455.1:n.1047+97G=
XM_011541154.1:c.1047+97G= XP_011539456.1:n.1047+97G=
XM_011541155.1:c.1047+97G= XP_011539457.1:n.1047+97G=
XM_011541156.1:c.1047+97G= XP_011539458.1:n.1047+97G=
XM_011541157.1:c.156+97G= XP_011539459.1:n.156+97G=
XM_011541154.2:c.1047+97G= XP_011539456.1:n.1047+97G=
NM_012387.3:c.1047+97G= MANE Select NP_036519.2:n.1047+97G=