Canonical Allele Identifier: CA338234212

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17660466C>G (hg19) ; chr1:g.17333971C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333971C>G , CM000663.2:g.17333971C>G	GRCh38
NC_000001.10:g.17660466C>G , CM000663.1:g.17660466C>G	GRCh37
NC_000001.9:g.17533053C>G	NCBI36
NG_023261.2:g.30782C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.302C>G MANE Select	ENSP00000364597.4:p.Thr101Ser
ENST00000375453.5:c.302C>G	ENSP00000364602.1:p.Thr101Ser
NM_012387.2:c.302C>G	NP_036519.2:p.Thr101Ser
XM_011541150.1:c.302C>G	XP_011539452.1:p.Thr101Ser
XM_011541151.1:c.302C>G	XP_011539453.1:p.Thr101Ser
XM_011541153.1:c.302C>G	XP_011539455.1:p.Thr101Ser
XM_011541154.1:c.302C>G	XP_011539456.1:p.Thr101Ser
XM_011541155.1:c.302C>G	XP_011539457.1:p.Thr101Ser
XM_011541156.1:c.302C>G	XP_011539458.1:p.Thr101Ser
XM_011541154.2:c.302C>G	XP_011539456.1:p.Thr101Ser
NM_012387.3:c.302C>G MANE Select	NP_036519.2:p.Thr101Ser