Canonical Allele Identifier: CA416411854
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17674501A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348006A>T , CM000663.2:g.17348006A>T GRCh38
NC_000001.10:g.17674501A>T , CM000663.1:g.17674501A>T GRCh37
NC_000001.9:g.17547088A>T NCBI36
NG_023261.2:g.44817A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1113A>T MANE Select ENSP00000364597.4:p.Pro371=
ENST00000468945.1:n.172A>T
ENST00000487048.5:n.80A>T
NM_012387.2:c.1113A>T NP_036519.2:p.Pro371=
XM_011541150.1:c.927A>T XP_011539452.1:p.Pro309=
XM_011541151.1:c.1113A>T XP_011539453.1:p.Pro371=
XM_011541152.1:c.576A>T XP_011539454.1:p.Pro192=
XM_011541153.1:c.1113A>T XP_011539455.1:p.Pro371=
XM_011541154.1:c.1113A>T XP_011539456.1:p.Pro371=
XM_011541155.1:c.1113A>T XP_011539457.1:p.Pro371=
XM_011541156.1:c.1113A>T XP_011539458.1:p.Pro371=
XM_011541157.1:c.222A>T XP_011539459.1:p.Pro74=
XM_011541154.2:c.1113A>T XP_011539456.1:p.Pro371=
NM_012387.3:c.1113A>T MANE Select NP_036519.2:p.Pro371=