Canonical Allele Identifier: CA338247452

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17672558C>T (hg19) ; chr1:g.17346063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17346063C>T , CM000663.2:g.17346063C>T	GRCh38
NC_000001.10:g.17672558C>T , CM000663.1:g.17672558C>T	GRCh37
NC_000001.9:g.17545145C>T	NCBI36
NG_023261.2:g.42874C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.971C>T MANE Select	ENSP00000364597.4:p.Thr324Ile
ENST00000468945.1:n.30C>T
NM_012387.2:c.971C>T	NP_036519.2:p.Thr324Ile
XM_011541150.1:c.785C>T	XP_011539452.1:p.Thr262Ile
XM_011541151.1:c.971C>T	XP_011539453.1:p.Thr324Ile
XM_011541152.1:c.434C>T	XP_011539454.1:p.Thr145Ile
XM_011541153.1:c.971C>T	XP_011539455.1:p.Thr324Ile
XM_011541154.1:c.971C>T	XP_011539456.1:p.Thr324Ile
XM_011541155.1:c.971C>T	XP_011539457.1:p.Thr324Ile
XM_011541156.1:c.971C>T	XP_011539458.1:p.Thr324Ile
XM_011541157.1:c.80C>T	XP_011539459.1:p.Thr27Ile
XM_011541154.2:c.971C>T	XP_011539456.1:p.Thr324Ile
NM_012387.3:c.971C>T MANE Select	NP_036519.2:p.Thr324Ile