Canonical Allele Identifier: CA640403

Gene: PADI4

Linked Data

• dbSNP Id: rs751866498
• ExAC: 1:17660427 C / T
• gnomAD v2: 1-17660427-C-T
• gnomAD v4: 1-17333932-C-T
• MyVariant Identifiers: chr1:g.17660427C>T (hg19) ; chr1:g.17333932C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333932C>T , CM000663.2:g.17333932C>T	GRCh38
NC_000001.10:g.17660427C>T , CM000663.1:g.17660427C>T	GRCh37
NC_000001.9:g.17533014C>T	NCBI36
NG_023261.2:g.30743C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.274-11C>T MANE Select	ENSP00000364597.4:n.274-11C>T
ENST00000375453.5:c.274-11C>T	ENSP00000364602.1:n.274-11C>T
NM_012387.2:c.274-11C>T	NP_036519.2:n.274-11C>T
XM_011541150.1:c.274-11C>T	XP_011539452.1:n.274-11C>T
XM_011541151.1:c.274-11C>T	XP_011539453.1:n.274-11C>T
XM_011541153.1:c.274-11C>T	XP_011539455.1:n.274-11C>T
XM_011541154.1:c.274-11C>T	XP_011539456.1:n.274-11C>T
XM_011541155.1:c.274-11C>T	XP_011539457.1:n.274-11C>T
XM_011541156.1:c.274-11C>T	XP_011539458.1:n.274-11C>T
XM_011541154.2:c.274-11C>T	XP_011539456.1:n.274-11C>T
NM_012387.3:c.274-11C>T MANE Select	NP_036519.2:n.274-11C>T