Canonical Allele Identifier: CA338234389

Gene: PADI4

Linked Data

• dbSNP Id: rs1194088205
• gnomAD v2: 1-17660481-C-T
• gnomAD v3: 1-17333986-C-T
• gnomAD v4: 1-17333986-C-T
• MyVariant Identifiers: chr1:g.17660481C>T (hg19) ; chr1:g.17333986C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333986C>T , CM000663.2:g.17333986C>T	GRCh38
NC_000001.10:g.17660481C>T , CM000663.1:g.17660481C>T	GRCh37
NC_000001.9:g.17533068C>T	NCBI36
NG_023261.2:g.30797C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.317C>T MANE Select	ENSP00000364597.4:p.Ala106Val
ENST00000375453.5:c.317C>T	ENSP00000364602.1:p.Ala106Val
NM_012387.2:c.317C>T	NP_036519.2:p.Ala106Val
XM_011541150.1:c.317C>T	XP_011539452.1:p.Ala106Val
XM_011541151.1:c.317C>T	XP_011539453.1:p.Ala106Val
XM_011541153.1:c.317C>T	XP_011539455.1:p.Ala106Val
XM_011541154.1:c.317C>T	XP_011539456.1:p.Ala106Val
XM_011541155.1:c.317C>T	XP_011539457.1:p.Ala106Val
XM_011541156.1:c.317C>T	XP_011539458.1:p.Ala106Val
XM_011541157.1:c.-396C>T	XP_011539459.1:n.-396C>T
XM_011541154.2:c.317C>T	XP_011539456.1:p.Ala106Val
NM_012387.3:c.317C>T MANE Select	NP_036519.2:p.Ala106Val