Canonical Allele Identifier: CA2643694401

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348057-ATGGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348063_17348067del , CM000663.2:g.17348063_17348067del	GRCh38
NC_000001.10:g.17674558_17674562del , CM000663.1:g.17674558_17674562del	GRCh37
NC_000001.9:g.17547145_17547149del	NCBI36
NG_023261.2:g.44874_44878del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+15_1155+19del MANE Select	ENSP00000364597.4:n.1155+15_1155+19del
ENST00000468945.1:n.229_233del
ENST00000487048.5:n.122+15_122+19del
NM_012387.2:c.1155+15_1155+19del	NP_036519.2:n.1155+15_1155+19del
XM_011541150.1:c.969+15_969+19del	XP_011539452.1:n.969+15_969+19del
XM_011541151.1:c.1155+15_1155+19del	XP_011539453.1:n.1155+15_1155+19del
XM_011541152.1:c.618+15_618+19del	XP_011539454.1:n.618+15_618+19del
XM_011541153.1:c.1155+15_1155+19del	XP_011539455.1:n.1155+15_1155+19del
XM_011541154.1:c.1155+15_1155+19del	XP_011539456.1:n.1155+15_1155+19del
XM_011541155.1:c.1155+15_1155+19del	XP_011539457.1:n.1155+15_1155+19del
XM_011541156.1:c.1155+15_1155+19del	XP_011539458.1:n.1155+15_1155+19del
XM_011541157.1:c.264+15_264+19del	XP_011539459.1:n.264+15_264+19del
XM_011541154.2:c.1155+15_1155+19del	XP_011539456.1:n.1155+15_1155+19del
NM_012387.3:c.1155+15_1155+19del MANE Select	NP_036519.2:n.1155+15_1155+19del