Canonical Allele Identifier: CA338249656

Gene: PADI4

Linked Data

• COSMIC: COSM254885
• MyVariant Identifiers: chr1:g.17674510A>T (hg19) ; chr1:g.17348015A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348015A>T , CM000663.2:g.17348015A>T	GRCh38
NC_000001.10:g.17674510A>T , CM000663.1:g.17674510A>T	GRCh37
NC_000001.9:g.17547097A>T	NCBI36
NG_023261.2:g.44826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1122A>T MANE Select	ENSP00000364597.4:p.Arg374Ser
ENST00000468945.1:n.181A>T
ENST00000487048.5:n.89A>T
NM_012387.2:c.1122A>T	NP_036519.2:p.Arg374Ser
XM_011541150.1:c.936A>T	XP_011539452.1:p.Arg312Ser
XM_011541151.1:c.1122A>T	XP_011539453.1:p.Arg374Ser
XM_011541152.1:c.585A>T	XP_011539454.1:p.Arg195Ser
XM_011541153.1:c.1122A>T	XP_011539455.1:p.Arg374Ser
XM_011541154.1:c.1122A>T	XP_011539456.1:p.Arg374Ser
XM_011541155.1:c.1122A>T	XP_011539457.1:p.Arg374Ser
XM_011541156.1:c.1122A>T	XP_011539458.1:p.Arg374Ser
XM_011541157.1:c.231A>T	XP_011539459.1:p.Arg77Ser
XM_011541154.2:c.1122A>T	XP_011539456.1:p.Arg374Ser
NM_012387.3:c.1122A>T MANE Select	NP_036519.2:p.Arg374Ser