Canonical Allele Identifier: CA338249660

Gene: PADI4

Linked Data

• dbSNP Id: rs2074549976
• MyVariant Identifiers: chr1:g.17674511G>T (hg19) ; chr1:g.17348016G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348016G>T , CM000663.2:g.17348016G>T	GRCh38
NC_000001.10:g.17674511G>T , CM000663.1:g.17674511G>T	GRCh37
NC_000001.9:g.17547098G>T	NCBI36
NG_023261.2:g.44827G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1123G>T MANE Select	ENSP00000364597.4:p.Gly375Cys
ENST00000468945.1:n.182G>T
ENST00000487048.5:n.90G>T
NM_012387.2:c.1123G>T	NP_036519.2:p.Gly375Cys
XM_011541150.1:c.937G>T	XP_011539452.1:p.Gly313Cys
XM_011541151.1:c.1123G>T	XP_011539453.1:p.Gly375Cys
XM_011541152.1:c.586G>T	XP_011539454.1:p.Gly196Cys
XM_011541153.1:c.1123G>T	XP_011539455.1:p.Gly375Cys
XM_011541154.1:c.1123G>T	XP_011539456.1:p.Gly375Cys
XM_011541155.1:c.1123G>T	XP_011539457.1:p.Gly375Cys
XM_011541156.1:c.1123G>T	XP_011539458.1:p.Gly375Cys
XM_011541157.1:c.232G>T	XP_011539459.1:p.Gly78Cys
XM_011541154.2:c.1123G>T	XP_011539456.1:p.Gly375Cys
NM_012387.3:c.1123G>T MANE Select	NP_036519.2:p.Gly375Cys