Canonical Allele Identifier: CA416418052

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17682523T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17356028T>C , CM000663.2:g.17356028T>C	GRCh38
NC_000001.10:g.17682523T>C , CM000663.1:g.17682523T>C	GRCh37
NC_000001.9:g.17555110T>C	NCBI36
NG_023261.2:g.52839T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1356T>C MANE Select	ENSP00000364597.4:p.Ser452=
ENST00000467001.1:n.257T>C
ENST00000487048.5:n.323T>C
NM_012387.2:c.1356T>C	NP_036519.2:p.Ser452=
XM_011541150.1:c.1170T>C	XP_011539452.1:p.Ser390=
XM_011541151.1:c.1156-329T>C	XP_011539453.1:n.1156-329T>C
XM_011541152.1:c.819T>C	XP_011539454.1:p.Ser273=
XM_011541154.1:c.*93T>C	XP_011539456.1:n.*93T>C
XM_011541156.1:c.*40T>C	XP_011539458.1:n.*40T>C
XM_011541157.1:c.465T>C	XP_011539459.1:p.Ser155=
XM_011541154.2:c.*93T>C	XP_011539456.1:n.*93T>C
NM_012387.3:c.1356T>C MANE Select	NP_036519.2:p.Ser452=