Canonical Allele Identifier: CA416403172
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17660482T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17333987T>A , CM000663.2:g.17333987T>A GRCh38
NC_000001.10:g.17660482T>A , CM000663.1:g.17660482T>A GRCh37
NC_000001.9:g.17533069T>A NCBI36
NG_023261.2:g.30798T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.318T>A MANE Select ENSP00000364597.4:p.Ala106=
ENST00000375453.5:c.318T>A ENSP00000364602.1:p.Ala106=
NM_012387.2:c.318T>A NP_036519.2:p.Ala106=
XM_011541150.1:c.318T>A XP_011539452.1:p.Ala106=
XM_011541151.1:c.318T>A XP_011539453.1:p.Ala106=
XM_011541153.1:c.318T>A XP_011539455.1:p.Ala106=
XM_011541154.1:c.318T>A XP_011539456.1:p.Ala106=
XM_011541155.1:c.318T>A XP_011539457.1:p.Ala106=
XM_011541156.1:c.318T>A XP_011539458.1:p.Ala106=
XM_011541157.1:c.-395T>A XP_011539459.1:n.-395T>A
XM_011541154.2:c.318T>A XP_011539456.1:p.Ala106=
NM_012387.3:c.318T>A MANE Select NP_036519.2:p.Ala106=