Canonical Allele Identifier: CA18635818

Gene: PADI4

Linked Data

• dbSNP Id: rs547031786
• gnomAD v3: 1-17334239-T-G
• gnomAD v4: 1-17334239-T-G
• MyVariant Identifiers: chr1:g.17660734T>G (hg19) ; chr1:g.17334239T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334239T>G , CM000663.2:g.17334239T>G	GRCh38
NC_000001.10:g.17660734T>G , CM000663.1:g.17660734T>G	GRCh37
NC_000001.9:g.17533321T>G	NCBI36
NG_023261.2:g.31050T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+230T>G MANE Select	ENSP00000364597.4:n.340+230T>G
ENST00000375453.5:c.341-85T>G	ENSP00000364602.1:n.341-85T>G
NM_012387.2:c.340+230T>G	NP_036519.2:n.340+230T>G
XM_011541150.1:c.340+230T>G	XP_011539452.1:n.340+230T>G
XM_011541151.1:c.340+230T>G	XP_011539453.1:n.340+230T>G
XM_011541152.1:c.-80+230T>G	XP_011539454.1:n.-80+230T>G
XM_011541153.1:c.340+230T>G	XP_011539455.1:n.340+230T>G
XM_011541154.1:c.340+230T>G	XP_011539456.1:n.340+230T>G
XM_011541155.1:c.340+230T>G	XP_011539457.1:n.340+230T>G
XM_011541156.1:c.340+230T>G	XP_011539458.1:n.340+230T>G
XM_011541157.1:c.-373+230T>G	XP_011539459.1:n.-373+230T>G
XM_011541154.2:c.340+230T>G	XP_011539456.1:n.340+230T>G
NM_012387.3:c.340+230T>G MANE Select	NP_036519.2:n.340+230T>G