Canonical Allele Identifier: CA416404781
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17662664G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336169G>A , CM000663.2:g.17336169G>A GRCh38
NC_000001.10:g.17662664G>A , CM000663.1:g.17662664G>A GRCh37
NC_000001.9:g.17535251G>A NCBI36
NG_023261.2:g.32980G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.351G>A MANE Select ENSP00000364597.4:p.Leu117=
NM_012387.2:c.351G>A NP_036519.2:p.Leu117=
XM_011541150.1:c.340+2160G>A XP_011539452.1:n.340+2160G>A
XM_011541151.1:c.351G>A XP_011539453.1:p.Leu117=
XM_011541152.1:c.-69G>A XP_011539454.1:n.-69G>A
XM_011541153.1:c.351G>A XP_011539455.1:p.Leu117=
XM_011541154.1:c.351G>A XP_011539456.1:p.Leu117=
XM_011541155.1:c.351G>A XP_011539457.1:p.Leu117=
XM_011541156.1:c.351G>A XP_011539458.1:p.Leu117=
XM_011541157.1:c.-362G>A XP_011539459.1:n.-362G>A
XM_011541154.2:c.351G>A XP_011539456.1:p.Leu117=
NM_012387.3:c.351G>A MANE Select NP_036519.2:p.Leu117=