Canonical Allele Identifier: CA338256210

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17682522G>C (hg19) ; chr1:g.17356027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17356027G>C , CM000663.2:g.17356027G>C	GRCh38
NC_000001.10:g.17682522G>C , CM000663.1:g.17682522G>C	GRCh37
NC_000001.9:g.17555109G>C	NCBI36
NG_023261.2:g.52838G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1355G>C MANE Select	ENSP00000364597.4:p.Ser452Thr
ENST00000467001.1:n.256G>C
ENST00000487048.5:n.322G>C
NM_012387.2:c.1355G>C	NP_036519.2:p.Ser452Thr
XM_011541150.1:c.1169G>C	XP_011539452.1:p.Ser390Thr
XM_011541151.1:c.1156-330G>C	XP_011539453.1:n.1156-330G>C
XM_011541152.1:c.818G>C	XP_011539454.1:p.Ser273Thr
XM_011541154.1:c.*92G>C	XP_011539456.1:n.*92G>C
XM_011541156.1:c.*39G>C	XP_011539458.1:n.*39G>C
XM_011541157.1:c.464G>C	XP_011539459.1:p.Ser155Thr
XM_011541154.2:c.*92G>C	XP_011539456.1:n.*92G>C
NM_012387.3:c.1355G>C MANE Select	NP_036519.2:p.Ser452Thr