Canonical Allele Identifier: CA999121617

Gene: PADI4

Linked Data

• gnomAD v3: 1-17333873-CATAGGAGGGGGTCCAGTGGGTGTTTGTTGA-C
• gnomAD v4: 1-17333873-CATAGGAGGGGGTCCAGTGGGTGTTTGTTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17333876_17333905del , CM000663.2:g.17333876_17333905del	GRCh38
NC_000001.10:g.17660371_17660400del , CM000663.1:g.17660371_17660400del	GRCh37
NC_000001.9:g.17532958_17532987del	NCBI36
NG_023261.2:g.30687_30716del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375448.4:c.274-67_274-38del MANE Select	ENSP00000364597.4:n.274-67_274-38del
ENST00000375453.5:c.274-67_274-38del	ENSP00000364602.1:n.274-67_274-38del
NM_012387.2:c.274-67_274-38del	NP_036519.2:n.274-67_274-38del
XM_011541150.1:c.274-67_274-38del	XP_011539452.1:n.274-67_274-38del
XM_011541151.1:c.274-67_274-38del	XP_011539453.1:n.274-67_274-38del
XM_011541153.1:c.274-67_274-38del	XP_011539455.1:n.274-67_274-38del
XM_011541154.1:c.274-67_274-38del	XP_011539456.1:n.274-67_274-38del
XM_011541155.1:c.274-67_274-38del	XP_011539457.1:n.274-67_274-38del
XM_011541156.1:c.274-67_274-38del	XP_011539458.1:n.274-67_274-38del
XM_011541154.2:c.274-67_274-38del	XP_011539456.1:n.274-67_274-38del
NM_012387.3:c.274-67_274-38del MANE Select	NP_036519.2:n.274-67_274-38del