Canonical Allele Identifier: CA338234571

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17660502T>A (hg19) ; chr1:g.17334007T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334007T>A , CM000663.2:g.17334007T>A	GRCh38
NC_000001.10:g.17660502T>A , CM000663.1:g.17660502T>A	GRCh37
NC_000001.9:g.17533089T>A	NCBI36
NG_023261.2:g.30818T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.338T>A MANE Select	ENSP00000364597.4:p.Val113Glu
ENST00000375453.5:c.338T>A	ENSP00000364602.1:p.Val113Glu
NM_012387.2:c.338T>A	NP_036519.2:p.Val113Glu
XM_011541150.1:c.338T>A	XP_011539452.1:p.Val113Glu
XM_011541151.1:c.338T>A	XP_011539453.1:p.Val113Glu
XM_011541152.1:c.-82T>A	XP_011539454.1:n.-82T>A
XM_011541153.1:c.338T>A	XP_011539455.1:p.Val113Glu
XM_011541154.1:c.338T>A	XP_011539456.1:p.Val113Glu
XM_011541155.1:c.338T>A	XP_011539457.1:p.Val113Glu
XM_011541156.1:c.338T>A	XP_011539458.1:p.Val113Glu
XM_011541157.1:c.-375T>A	XP_011539459.1:n.-375T>A
XM_011541154.2:c.338T>A	XP_011539456.1:p.Val113Glu
NM_012387.3:c.338T>A MANE Select	NP_036519.2:p.Val113Glu