Canonical Allele Identifier: CA2643694413
Gene: PADI4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348066_17348079del , CM000663.2:g.17348066_17348079del GRCh38
NC_000001.10:g.17674561_17674574del , CM000663.1:g.17674561_17674574del GRCh37
NC_000001.9:g.17547148_17547161del NCBI36
NG_023261.2:g.44877_44890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+18_1155+31del MANE Select ENSP00000364597.4:n.1155+18_1155+31del
ENST00000468945.1:n.232_245del
ENST00000487048.5:n.122+18_122+31del
NM_012387.2:c.1155+18_1155+31del NP_036519.2:n.1155+18_1155+31del
XM_011541150.1:c.969+18_969+31del XP_011539452.1:n.969+18_969+31del
XM_011541151.1:c.1155+18_1155+31del XP_011539453.1:n.1155+18_1155+31del
XM_011541152.1:c.618+18_618+31del XP_011539454.1:n.618+18_618+31del
XM_011541153.1:c.1155+18_1155+31del XP_011539455.1:n.1155+18_1155+31del
XM_011541154.1:c.1155+18_1155+31del XP_011539456.1:n.1155+18_1155+31del
XM_011541155.1:c.1155+18_1155+31del XP_011539457.1:n.1155+18_1155+31del
XM_011541156.1:c.1155+18_1155+31del XP_011539458.1:n.1155+18_1155+31del
XM_011541157.1:c.264+18_264+31del XP_011539459.1:n.264+18_264+31del
XM_011541154.2:c.1155+18_1155+31del XP_011539456.1:n.1155+18_1155+31del
NM_012387.3:c.1155+18_1155+31del MANE Select NP_036519.2:n.1155+18_1155+31del