Canonical Allele Identifier: CA2643694434

Gene: PADI4

Linked Data

• gnomAD v4: 1-17348106-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17348110_17348112del , CM000663.2:g.17348110_17348112del	GRCh38
NC_000001.10:g.17674605_17674607del , CM000663.1:g.17674605_17674607del	GRCh37
NC_000001.9:g.17547192_17547194del	NCBI36
NG_023261.2:g.44921_44923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375448.4:c.1155+62_1155+64del MANE Select	ENSP00000364597.4:n.1155+62_1155+64del
ENST00000468945.1:n.276_278del
ENST00000487048.5:n.122+62_122+64del
NM_012387.2:c.1155+62_1155+64del	NP_036519.2:n.1155+62_1155+64del
XM_011541150.1:c.969+62_969+64del	XP_011539452.1:n.969+62_969+64del
XM_011541151.1:c.1155+62_1155+64del	XP_011539453.1:n.1155+62_1155+64del
XM_011541152.1:c.618+62_618+64del	XP_011539454.1:n.618+62_618+64del
XM_011541153.1:c.1155+62_1155+64del	XP_011539455.1:n.1155+62_1155+64del
XM_011541154.1:c.1155+62_1155+64del	XP_011539456.1:n.1155+62_1155+64del
XM_011541155.1:c.1155+62_1155+64del	XP_011539457.1:n.1155+62_1155+64del
XM_011541156.1:c.1155+62_1155+64del	XP_011539458.1:n.1155+62_1155+64del
XM_011541157.1:c.264+62_264+64del	XP_011539459.1:n.264+62_264+64del
XM_011541154.2:c.1155+62_1155+64del	XP_011539456.1:n.1155+62_1155+64del
NM_012387.3:c.1155+62_1155+64del MANE Select	NP_036519.2:n.1155+62_1155+64del