Canonical Allele Identifier: CA338249500
Gene: PADI4 HGNC NCBI

Linked Data

gnomAD v4: 1-17347957-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17347957G>A , CM000663.2:g.17347957G>A GRCh38
NC_000001.10:g.17674452G>A , CM000663.1:g.17674452G>A GRCh37
NC_000001.9:g.17547039G>A NCBI36
NG_023261.2:g.44768G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1064G>A MANE Select ENSP00000364597.4:p.Gly355Asp
ENST00000468945.1:n.123G>A
ENST00000487048.5:n.31G>A
NM_012387.2:c.1064G>A NP_036519.2:p.Gly355Asp
XM_011541150.1:c.878G>A XP_011539452.1:p.Gly293Asp
XM_011541151.1:c.1064G>A XP_011539453.1:p.Gly355Asp
XM_011541152.1:c.527G>A XP_011539454.1:p.Gly176Asp
XM_011541153.1:c.1064G>A XP_011539455.1:p.Gly355Asp
XM_011541154.1:c.1064G>A XP_011539456.1:p.Gly355Asp
XM_011541155.1:c.1064G>A XP_011539457.1:p.Gly355Asp
XM_011541156.1:c.1064G>A XP_011539458.1:p.Gly355Asp
XM_011541157.1:c.173G>A XP_011539459.1:p.Gly58Asp
XM_011541154.2:c.1064G>A XP_011539456.1:p.Gly355Asp
NM_012387.3:c.1064G>A MANE Select NP_036519.2:p.Gly355Asp