Canonical Allele Identifier: CA521042345

Gene: PADI4

Linked Data

• dbSNP Id: rs1289784293
• gnomAD v2: 1-17660803-T-TG
• MyVariant Identifiers: chr1:g.17660803_17660804insG (hg19) ; chr1:g.17334308_17334309insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17334308_17334309insG , CM000663.2:g.17334308_17334309insG	GRCh38
NC_000001.10:g.17660803_17660804insG , CM000663.1:g.17660803_17660804insG	GRCh37
NC_000001.9:g.17533390_17533391insG	NCBI36
NG_023261.2:g.31119_31120insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.340+299_340+300insG MANE Select	ENSP00000364597.4:n.340+299_340+300insG
ENST00000375453.5:c.341-16_341-15insG	ENSP00000364602.1:n.341-16_341-15insG
NM_012387.2:c.340+299_340+300insG	NP_036519.2:n.340+299_340+300insG
XM_011541150.1:c.340+299_340+300insG	XP_011539452.1:n.340+299_340+300insG
XM_011541151.1:c.340+299_340+300insG	XP_011539453.1:n.340+299_340+300insG
XM_011541152.1:c.-80+299_-80+300insG	XP_011539454.1:n.-80+299_-80+300insG
XM_011541153.1:c.340+299_340+300insG	XP_011539455.1:n.340+299_340+300insG
XM_011541154.1:c.340+299_340+300insG	XP_011539456.1:n.340+299_340+300insG
XM_011541155.1:c.340+299_340+300insG	XP_011539457.1:n.340+299_340+300insG
XM_011541156.1:c.340+299_340+300insG	XP_011539458.1:n.340+299_340+300insG
XM_011541157.1:c.-373+299_-373+300insG	XP_011539459.1:n.-373+299_-373+300insG
XM_011541154.2:c.340+299_340+300insG	XP_011539456.1:n.340+299_340+300insG
NM_012387.3:c.340+299_340+300insG MANE Select	NP_036519.2:n.340+299_340+300insG