Canonical Allele Identifier: CA521042947

Gene: PADI4

Linked Data

• dbSNP Id: rs1312450597
• gnomAD v2: 1-17662540-C-T
• gnomAD v3: 1-17336045-C-T
• gnomAD v4: 1-17336045-C-T
• MyVariant Identifiers: chr1:g.17662540C>T (hg19) ; chr1:g.17336045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17336045C>T , CM000663.2:g.17336045C>T	GRCh38
NC_000001.10:g.17662540C>T , CM000663.1:g.17662540C>T	GRCh37
NC_000001.9:g.17535127C>T	NCBI36
NG_023261.2:g.32856C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.341-114C>T MANE Select	ENSP00000364597.4:n.341-114C>T
NM_012387.2:c.341-114C>T	NP_036519.2:n.341-114C>T
XM_011541150.1:c.340+2036C>T	XP_011539452.1:n.340+2036C>T
XM_011541151.1:c.341-114C>T	XP_011539453.1:n.341-114C>T
XM_011541152.1:c.-79-114C>T	XP_011539454.1:n.-79-114C>T
XM_011541153.1:c.341-114C>T	XP_011539455.1:n.341-114C>T
XM_011541154.1:c.341-114C>T	XP_011539456.1:n.341-114C>T
XM_011541155.1:c.341-114C>T	XP_011539457.1:n.341-114C>T
XM_011541156.1:c.341-114C>T	XP_011539458.1:n.341-114C>T
XM_011541157.1:c.-372-114C>T	XP_011539459.1:n.-372-114C>T
XM_011541154.2:c.341-114C>T	XP_011539456.1:n.341-114C>T
NM_012387.3:c.341-114C>T MANE Select	NP_036519.2:n.341-114C>T