Canonical Allele Identifier: CA338249536

Gene: PADI4

Linked Data

• COSMIC: COSM75829
• MyVariant Identifiers: chr1:g.17674461A>T (hg19) ; chr1:g.17347966A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347966A>T , CM000663.2:g.17347966A>T	GRCh38
NC_000001.10:g.17674461A>T , CM000663.1:g.17674461A>T	GRCh37
NC_000001.9:g.17547048A>T	NCBI36
NG_023261.2:g.44777A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1073A>T MANE Select	ENSP00000364597.4:p.Gln358Leu
ENST00000468945.1:n.132A>T
ENST00000487048.5:n.40A>T
NM_012387.2:c.1073A>T	NP_036519.2:p.Gln358Leu
XM_011541150.1:c.887A>T	XP_011539452.1:p.Gln296Leu
XM_011541151.1:c.1073A>T	XP_011539453.1:p.Gln358Leu
XM_011541152.1:c.536A>T	XP_011539454.1:p.Gln179Leu
XM_011541153.1:c.1073A>T	XP_011539455.1:p.Gln358Leu
XM_011541154.1:c.1073A>T	XP_011539456.1:p.Gln358Leu
XM_011541155.1:c.1073A>T	XP_011539457.1:p.Gln358Leu
XM_011541156.1:c.1073A>T	XP_011539458.1:p.Gln358Leu
XM_011541157.1:c.182A>T	XP_011539459.1:p.Gln61Leu
XM_011541154.2:c.1073A>T	XP_011539456.1:p.Gln358Leu
NM_012387.3:c.1073A>T MANE Select	NP_036519.2:p.Gln358Leu