Canonical Allele Identifier: CA1156200661

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348426G= , CM000663.2:g.17348426G=	GRCh38
NC_000001.10:g.17674921G= , CM000663.1:g.17674921G=	GRCh37
NC_000001.9:g.17547508G=	NCBI36
NG_023261.2:g.45237G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+378G= MANE Select	ENSP00000364597.4:n.1155+378G=
ENST00000487048.5:n.122+378G=
NM_012387.2:c.1155+378G=	NP_036519.2:n.1155+378G=
XM_011541150.1:c.969+378G=	XP_011539452.1:n.969+378G=
XM_011541151.1:c.1155+378G=	XP_011539453.1:n.1155+378G=
XM_011541152.1:c.618+378G=	XP_011539454.1:n.618+378G=
XM_011541153.1:c.1156-274G=	XP_011539455.1:n.1156-274G=
XM_011541154.1:c.1156-274G=	XP_011539456.1:n.1156-274G=
XM_011541155.1:c.1155+378G=	XP_011539457.1:n.1155+378G=
XM_011541156.1:c.1155+378G=	XP_011539458.1:n.1155+378G=
XM_011541157.1:c.264+378G=	XP_011539459.1:n.264+378G=
XM_011541154.2:c.1156-274G=	XP_011539456.1:n.1156-274G=
NM_012387.3:c.1155+378G= MANE Select	NP_036519.2:n.1155+378G=