Canonical Allele Identifier: CA416418109
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17682532G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17356037G>A , CM000663.2:g.17356037G>A GRCh38
NC_000001.10:g.17682532G>A , CM000663.1:g.17682532G>A GRCh37
NC_000001.9:g.17555119G>A NCBI36
NG_023261.2:g.52848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1365G>A MANE Select ENSP00000364597.4:p.Gln455=
ENST00000467001.1:n.266G>A
ENST00000487048.5:n.332G>A
NM_012387.2:c.1365G>A NP_036519.2:p.Gln455=
XM_011541150.1:c.1179G>A XP_011539452.1:p.Gln393=
XM_011541151.1:c.1156-320G>A XP_011539453.1:n.1156-320G>A
XM_011541152.1:c.828G>A XP_011539454.1:p.Gln276=
XM_011541154.1:c.*102G>A XP_011539456.1:n.*102G>A
XM_011541156.1:c.*49G>A XP_011539458.1:n.*49G>A
XM_011541157.1:c.474G>A XP_011539459.1:p.Gln158=
XM_011541154.2:c.*102G>A XP_011539456.1:n.*102G>A
NM_012387.3:c.1365G>A MANE Select NP_036519.2:p.Gln455=