Canonical Allele Identifier: CA338249630

Gene: PADI4

Linked Data

• dbSNP Id: rs1419329579
• MyVariant Identifiers: chr1:g.17674497C>G (hg19) ; chr1:g.17348002C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348002C>G , CM000663.2:g.17348002C>G	GRCh38
NC_000001.10:g.17674497C>G , CM000663.1:g.17674497C>G	GRCh37
NC_000001.9:g.17547084C>G	NCBI36
NG_023261.2:g.44813C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1109C>G MANE Select	ENSP00000364597.4:p.Ser370Cys
ENST00000468945.1:n.168C>G
ENST00000487048.5:n.76C>G
NM_012387.2:c.1109C>G	NP_036519.2:p.Ser370Cys
XM_011541150.1:c.923C>G	XP_011539452.1:p.Ser308Cys
XM_011541151.1:c.1109C>G	XP_011539453.1:p.Ser370Cys
XM_011541152.1:c.572C>G	XP_011539454.1:p.Ser191Cys
XM_011541153.1:c.1109C>G	XP_011539455.1:p.Ser370Cys
XM_011541154.1:c.1109C>G	XP_011539456.1:p.Ser370Cys
XM_011541155.1:c.1109C>G	XP_011539457.1:p.Ser370Cys
XM_011541156.1:c.1109C>G	XP_011539458.1:p.Ser370Cys
XM_011541157.1:c.218C>G	XP_011539459.1:p.Ser73Cys
XM_011541154.2:c.1109C>G	XP_011539456.1:p.Ser370Cys
NM_012387.3:c.1109C>G MANE Select	NP_036519.2:p.Ser370Cys