Canonical Allele Identifier: CA2643694421

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348077-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348078dup , CM000663.2:g.17348078dup	GRCh38
NC_000001.10:g.17674573dup , CM000663.1:g.17674573dup	GRCh37
NC_000001.9:g.17547160dup	NCBI36
NG_023261.2:g.44889dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+30dup MANE Select	ENSP00000364597.4:n.1155+30dup
ENST00000468945.1:n.244dup
ENST00000487048.5:n.122+30dup
NM_012387.2:c.1155+30dup	NP_036519.2:n.1155+30dup
XM_011541150.1:c.969+30dup	XP_011539452.1:n.969+30dup
XM_011541151.1:c.1155+30dup	XP_011539453.1:n.1155+30dup
XM_011541152.1:c.618+30dup	XP_011539454.1:n.618+30dup
XM_011541153.1:c.1155+30dup	XP_011539455.1:n.1155+30dup
XM_011541154.1:c.1155+30dup	XP_011539456.1:n.1155+30dup
XM_011541155.1:c.1155+30dup	XP_011539457.1:n.1155+30dup
XM_011541156.1:c.1155+30dup	XP_011539458.1:n.1155+30dup
XM_011541157.1:c.264+30dup	XP_011539459.1:n.264+30dup
XM_011541154.2:c.1155+30dup	XP_011539456.1:n.1155+30dup
NM_012387.3:c.1155+30dup MANE Select	NP_036519.2:n.1155+30dup