Canonical Allele Identifier: CA338236606

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17662722G>T (hg19) ; chr1:g.17336227G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336227G>T , CM000663.2:g.17336227G>T	GRCh38
NC_000001.10:g.17662722G>T , CM000663.1:g.17662722G>T	GRCh37
NC_000001.9:g.17535309G>T	NCBI36
NG_023261.2:g.33038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.408+1G>T MANE Select	ENSP00000364597.4:n.408+1G>T
NM_012387.2:c.408+1G>T	NP_036519.2:n.408+1G>T
XM_011541150.1:c.340+2218G>T	XP_011539452.1:n.340+2218G>T
XM_011541151.1:c.408+1G>T	XP_011539453.1:n.408+1G>T
XM_011541152.1:c.-12+1G>T	XP_011539454.1:n.-12+1G>T
XM_011541153.1:c.408+1G>T	XP_011539455.1:n.408+1G>T
XM_011541154.1:c.408+1G>T	XP_011539456.1:n.408+1G>T
XM_011541155.1:c.408+1G>T	XP_011539457.1:n.408+1G>T
XM_011541156.1:c.408+1G>T	XP_011539458.1:n.408+1G>T
XM_011541157.1:c.-305+1G>T	XP_011539459.1:n.-305+1G>T
XM_011541154.2:c.408+1G>T	XP_011539456.1:n.408+1G>T
NM_012387.3:c.408+1G>T MANE Select	NP_036519.2:n.408+1G>T