Canonical Allele Identifier: CA338236277

Gene: PADI4

Linked Data

• dbSNP Id: rs1341157027
• MyVariant Identifiers: chr1:g.17662675T>G (hg19) ; chr1:g.17336180T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336180T>G , CM000663.2:g.17336180T>G	GRCh38
NC_000001.10:g.17662675T>G , CM000663.1:g.17662675T>G	GRCh37
NC_000001.9:g.17535262T>G	NCBI36
NG_023261.2:g.32991T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.362T>G MANE Select	ENSP00000364597.4:p.Ile121Ser
NM_012387.2:c.362T>G	NP_036519.2:p.Ile121Ser
XM_011541150.1:c.340+2171T>G	XP_011539452.1:n.340+2171T>G
XM_011541151.1:c.362T>G	XP_011539453.1:p.Ile121Ser
XM_011541152.1:c.-58T>G	XP_011539454.1:n.-58T>G
XM_011541153.1:c.362T>G	XP_011539455.1:p.Ile121Ser
XM_011541154.1:c.362T>G	XP_011539456.1:p.Ile121Ser
XM_011541155.1:c.362T>G	XP_011539457.1:p.Ile121Ser
XM_011541156.1:c.362T>G	XP_011539458.1:p.Ile121Ser
XM_011541157.1:c.-351T>G	XP_011539459.1:n.-351T>G
XM_011541154.2:c.362T>G	XP_011539456.1:p.Ile121Ser
NM_012387.3:c.362T>G MANE Select	NP_036519.2:p.Ile121Ser