Canonical Allele Identifier: CA640790
Gene: PADI4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2240335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348042C>A , CM000663.2:g.17348042C>A GRCh38
NC_000001.10:g.17674537C>A , CM000663.1:g.17674537C>A GRCh37
NC_000001.9:g.17547124C>A NCBI36
NG_023261.2:g.44853C>A

Transcript Alleles

HGVS Amino-acid change
NM_012387.2:c.1149C>A VV NP_036519.2:p.Arg383=
XM_011541150.1:c.963C>A XP_011539452.1:p.Arg321=
XM_011541151.1:c.1149C>A XP_011539453.1:p.Arg383=
XM_011541152.1:c.612C>A XP_011539454.1:p.Arg204=
XM_011541153.1:c.1149C>A XP_011539455.1:p.Arg383=
XM_011541154.1:c.1149C>A XP_011539456.1:p.Arg383=
XM_011541155.1:c.1149C>A XP_011539457.1:p.Arg383=
XM_011541156.1:c.1149C>A XP_011539458.1:p.Arg383=
XM_011541157.1:c.258C>A XP_011539459.1:p.Arg86=
XM_011541154.2:c.1149C>A XP_011539456.1:p.Arg383=
NM_012387.3:c.1149C>A VV MANE Preferred NP_036519.2:p.Arg383=
ENST00000375448.4:c.1149C>A ENSP00000364597.4:p.Arg383=
ENST00000468945.1:n.208C>A
ENST00000487048.5:n.116C>A