Canonical Allele Identifier: CA416418129
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17682535G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17356040G>A , CM000663.2:g.17356040G>A GRCh38
NC_000001.10:g.17682535G>A , CM000663.1:g.17682535G>A GRCh37
NC_000001.9:g.17555122G>A NCBI36
NG_023261.2:g.52851G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1368G>A MANE Select ENSP00000364597.4:p.Val456=
ENST00000467001.1:n.269G>A
ENST00000487048.5:n.335G>A
NM_012387.2:c.1368G>A NP_036519.2:p.Val456=
XM_011541150.1:c.1182G>A XP_011539452.1:p.Val394=
XM_011541151.1:c.1156-317G>A XP_011539453.1:n.1156-317G>A
XM_011541152.1:c.831G>A XP_011539454.1:p.Val277=
XM_011541154.1:c.*105G>A XP_011539456.1:n.*105G>A
XM_011541156.1:c.*52G>A XP_011539458.1:n.*52G>A
XM_011541157.1:c.477G>A XP_011539459.1:p.Val159=
XM_011541154.2:c.*105G>A XP_011539456.1:n.*105G>A
NM_012387.3:c.1368G>A MANE Select NP_036519.2:p.Val456=