Canonical Allele Identifier: CA1156197952

Gene: PADI4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346145T= , CM000663.2:g.17346145T=	GRCh38
NC_000001.10:g.17672640T= , CM000663.1:g.17672640T=	GRCh37
NC_000001.9:g.17545227T=	NCBI36
NG_023261.2:g.42956T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.1047+6T= MANE Select	ENSP00000364597.4:n.1047+6T=
ENST00000468945.1:n.106+6T=
NM_012387.2:c.1047+6T=	NP_036519.2:n.1047+6T=
XM_011541150.1:c.861+6T=	XP_011539452.1:n.861+6T=
XM_011541151.1:c.1047+6T=	XP_011539453.1:n.1047+6T=
XM_011541152.1:c.510+6T=	XP_011539454.1:n.510+6T=
XM_011541153.1:c.1047+6T=	XP_011539455.1:n.1047+6T=
XM_011541154.1:c.1047+6T=	XP_011539456.1:n.1047+6T=
XM_011541155.1:c.1047+6T=	XP_011539457.1:n.1047+6T=
XM_011541156.1:c.1047+6T=	XP_011539458.1:n.1047+6T=
XM_011541157.1:c.156+6T=	XP_011539459.1:n.156+6T=
XM_011541154.2:c.1047+6T=	XP_011539456.1:n.1047+6T=
NM_012387.3:c.1047+6T= MANE Select	NP_036519.2:n.1047+6T=