Canonical Allele Identifier: CA338249468

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17674444G>T (hg19) ; chr1:g.17347949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17347949G>T , CM000663.2:g.17347949G>T	GRCh38
NC_000001.10:g.17674444G>T , CM000663.1:g.17674444G>T	GRCh37
NC_000001.9:g.17547031G>T	NCBI36
NG_023261.2:g.44760G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.1056G>T MANE Select	ENSP00000364597.4:p.Met352Ile
ENST00000468945.1:n.115G>T
ENST00000487048.5:n.23G>T
NM_012387.2:c.1056G>T	NP_036519.2:p.Met352Ile
XM_011541150.1:c.870G>T	XP_011539452.1:p.Met290Ile
XM_011541151.1:c.1056G>T	XP_011539453.1:p.Met352Ile
XM_011541152.1:c.519G>T	XP_011539454.1:p.Met173Ile
XM_011541153.1:c.1056G>T	XP_011539455.1:p.Met352Ile
XM_011541154.1:c.1056G>T	XP_011539456.1:p.Met352Ile
XM_011541155.1:c.1056G>T	XP_011539457.1:p.Met352Ile
XM_011541156.1:c.1056G>T	XP_011539458.1:p.Met352Ile
XM_011541157.1:c.165G>T	XP_011539459.1:p.Met55Ile
XM_011541154.2:c.1056G>T	XP_011539456.1:p.Met352Ile
NM_012387.3:c.1056G>T MANE Select	NP_036519.2:p.Met352Ile