Canonical Allele Identifier: CA416418069

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17682526C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17356031C>G , CM000663.2:g.17356031C>G	GRCh38
NC_000001.10:g.17682526C>G , CM000663.1:g.17682526C>G	GRCh37
NC_000001.9:g.17555113C>G	NCBI36
NG_023261.2:g.52842C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1359C>G MANE Select	ENSP00000364597.4:p.Ala453=
ENST00000467001.1:n.260C>G
ENST00000487048.5:n.326C>G
NM_012387.2:c.1359C>G	NP_036519.2:p.Ala453=
XM_011541150.1:c.1173C>G	XP_011539452.1:p.Ala391=
XM_011541151.1:c.1156-326C>G	XP_011539453.1:n.1156-326C>G
XM_011541152.1:c.822C>G	XP_011539454.1:p.Ala274=
XM_011541154.1:c.*96C>G	XP_011539456.1:n.*96C>G
XM_011541156.1:c.*43C>G	XP_011539458.1:n.*43C>G
XM_011541157.1:c.468C>G	XP_011539459.1:p.Ala156=
XM_011541154.2:c.*96C>G	XP_011539456.1:n.*96C>G
NM_012387.3:c.1359C>G MANE Select	NP_036519.2:p.Ala453=