Canonical Allele Identifier: CA416405027
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17662694G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336199G>T , CM000663.2:g.17336199G>T GRCh38
NC_000001.10:g.17662694G>T , CM000663.1:g.17662694G>T GRCh37
NC_000001.9:g.17535281G>T NCBI36
NG_023261.2:g.33010G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.381G>T MANE Select ENSP00000364597.4:p.Val127=
NM_012387.2:c.381G>T NP_036519.2:p.Val127=
XM_011541150.1:c.340+2190G>T XP_011539452.1:n.340+2190G>T
XM_011541151.1:c.381G>T XP_011539453.1:p.Val127=
XM_011541152.1:c.-39G>T XP_011539454.1:n.-39G>T
XM_011541153.1:c.381G>T XP_011539455.1:p.Val127=
XM_011541154.1:c.381G>T XP_011539456.1:p.Val127=
XM_011541155.1:c.381G>T XP_011539457.1:p.Val127=
XM_011541156.1:c.381G>T XP_011539458.1:p.Val127=
XM_011541157.1:c.-332G>T XP_011539459.1:n.-332G>T
XM_011541154.2:c.381G>T XP_011539456.1:p.Val127=
NM_012387.3:c.381G>T MANE Select NP_036519.2:p.Val127=