Canonical Allele Identifier: CA416405102
Gene: PADI4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17662709T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336214T>C , CM000663.2:g.17336214T>C GRCh38
NC_000001.10:g.17662709T>C , CM000663.1:g.17662709T>C GRCh37
NC_000001.9:g.17535296T>C NCBI36
NG_023261.2:g.33025T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.396T>C MANE Select ENSP00000364597.4:p.Ala132=
NM_012387.2:c.396T>C NP_036519.2:p.Ala132=
XM_011541150.1:c.340+2205T>C XP_011539452.1:n.340+2205T>C
XM_011541151.1:c.396T>C XP_011539453.1:p.Ala132=
XM_011541152.1:c.-24T>C XP_011539454.1:n.-24T>C
XM_011541153.1:c.396T>C XP_011539455.1:p.Ala132=
XM_011541154.1:c.396T>C XP_011539456.1:p.Ala132=
XM_011541155.1:c.396T>C XP_011539457.1:p.Ala132=
XM_011541156.1:c.396T>C XP_011539458.1:p.Ala132=
XM_011541157.1:c.-317T>C XP_011539459.1:n.-317T>C
XM_011541154.2:c.396T>C XP_011539456.1:p.Ala132=
NM_012387.3:c.396T>C MANE Select NP_036519.2:p.Ala132=