Canonical Allele Identifier: CA338232284

Gene: PADI4

Linked Data

• MyVariant Identifiers: chr1:g.17657628G>C (hg19) ; chr1:g.17331133G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17331133G>C , CM000663.2:g.17331133G>C	GRCh38
NC_000001.10:g.17657628G>C , CM000663.1:g.17657628G>C	GRCh37
NC_000001.9:g.17530215G>C	NCBI36
NG_023261.2:g.27944G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.257G>C MANE Select	ENSP00000364597.4:p.Ser86Thr
ENST00000375453.5:c.257G>C	ENSP00000364602.1:p.Ser86Thr
ENST00000624583.1:c.166+498C>G	ENSP00000485570.1:n.166+498C>G
NM_012387.2:c.257G>C	NP_036519.2:p.Ser86Thr
XM_011541150.1:c.257G>C	XP_011539452.1:p.Ser86Thr
XM_011541151.1:c.257G>C	XP_011539453.1:p.Ser86Thr
XM_011541153.1:c.257G>C	XP_011539455.1:p.Ser86Thr
XM_011541154.1:c.257G>C	XP_011539456.1:p.Ser86Thr
XM_011541155.1:c.257G>C	XP_011539457.1:p.Ser86Thr
XM_011541156.1:c.257G>C	XP_011539458.1:p.Ser86Thr
XM_011541154.2:c.257G>C	XP_011539456.1:p.Ser86Thr
NM_012387.3:c.257G>C MANE Select	NP_036519.2:p.Ser86Thr