Canonical Allele Identifier: CA416410060

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17672637A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346142A>G , CM000663.2:g.17346142A>G	GRCh38
NC_000001.10:g.17672637A>G , CM000663.1:g.17672637A>G	GRCh37
NC_000001.9:g.17545224A>G	NCBI36
NG_023261.2:g.42953A>G

Transcript Alleles

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