Canonical Allele Identifier: CA1139884578
Community Standard Title: NM_012387.3(PADI4):c.526+751G=
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17338906G= , CM000663.2:g.17338906G= GRCh38
NC_000001.10:g.17665401G= , CM000663.1:g.17665401G= GRCh37
NC_000001.9:g.17537988G= NCBI36
NG_023261.2:g.35717G=

Transcript Alleles

HGVS Amino-acid Change
NM_012387.3:c.526+751G= MANE Select NP_036519.2:n.526+751G=
ENST00000375448.4:c.526+751G= MANE Select ENSP00000364597.4:n.526+751G=
NM_012387.2:c.526+751G= NP_036519.2:n.526+751G=
XM_011541150.1:c.341-782G= XP_011539452.1:n.341-782G=
XM_011541151.1:c.526+751G= XP_011539453.1:n.526+751G=
XM_011541152.1:c.-11-782G= XP_011539454.1:n.-11-782G=
XM_011541153.1:c.526+751G= XP_011539455.1:n.526+751G=
XM_011541154.1:c.526+751G= XP_011539456.1:n.526+751G=
XM_011541154.2:c.526+751G= XP_011539456.1:n.526+751G=
XM_011541155.1:c.526+751G= XP_011539457.1:n.526+751G=
XM_011541156.1:c.526+751G= XP_011539458.1:n.526+751G=
XM_011541157.1:c.-187+751G= XP_011539459.1:n.-187+751G=