Canonical Allele Identifier: CA1143649401
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17333960C= , CM000663.2:g.17333960C= GRCh38
NC_000001.10:g.17660455C= , CM000663.1:g.17660455C= GRCh37
NC_000001.9:g.17533042C= NCBI36
NG_023261.2:g.30771C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.291C= MANE Select ENSP00000364597.4:p.Tyr97=
ENST00000375453.5:c.291C= ENSP00000364602.1:p.Tyr97=
NM_012387.2:c.291C= NP_036519.2:p.Tyr97=
XM_011541150.1:c.291C= XP_011539452.1:p.Tyr97=
XM_011541151.1:c.291C= XP_011539453.1:p.Tyr97=
XM_011541153.1:c.291C= XP_011539455.1:p.Tyr97=
XM_011541154.1:c.291C= XP_011539456.1:p.Tyr97=
XM_011541155.1:c.291C= XP_011539457.1:p.Tyr97=
XM_011541156.1:c.291C= XP_011539458.1:p.Tyr97=
XM_011541154.2:c.291C= XP_011539456.1:p.Tyr97=
NM_012387.3:c.291C= MANE Select NP_036519.2:p.Tyr97=