Canonical Allele Identifier: CA891204341

Gene: PADI4

Linked Data

• dbSNP Id: rs1321510396
• gnomAD v4: 1-17334181-A-T
• MyVariant Identifiers: chr1:g.17660676A>T (hg19) ; chr1:g.17334181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334181A>T , CM000663.2:g.17334181A>T	GRCh38
NC_000001.10:g.17660676A>T , CM000663.1:g.17660676A>T	GRCh37
NC_000001.9:g.17533263A>T	NCBI36
NG_023261.2:g.30992A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+172A>T MANE Select	ENSP00000364597.4:n.340+172A>T
ENST00000375453.5:c.341-143A>T	ENSP00000364602.1:n.341-143A>T
NM_012387.2:c.340+172A>T	NP_036519.2:n.340+172A>T
XM_011541150.1:c.340+172A>T	XP_011539452.1:n.340+172A>T
XM_011541151.1:c.340+172A>T	XP_011539453.1:n.340+172A>T
XM_011541152.1:c.-80+172A>T	XP_011539454.1:n.-80+172A>T
XM_011541153.1:c.340+172A>T	XP_011539455.1:n.340+172A>T
XM_011541154.1:c.340+172A>T	XP_011539456.1:n.340+172A>T
XM_011541155.1:c.340+172A>T	XP_011539457.1:n.340+172A>T
XM_011541156.1:c.340+172A>T	XP_011539458.1:n.340+172A>T
XM_011541157.1:c.-373+172A>T	XP_011539459.1:n.-373+172A>T
XM_011541154.2:c.340+172A>T	XP_011539456.1:n.340+172A>T
NM_012387.3:c.340+172A>T MANE Select	NP_036519.2:n.340+172A>T