Canonical Allele Identifier: CA1156200648
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs2074558821

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348414del , CM000663.2:g.17348414del GRCh38
NC_000001.10:g.17674909del , CM000663.1:g.17674909del GRCh37
NC_000001.9:g.17547496del NCBI36
NG_023261.2:g.45225del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+366del MANE Select ENSP00000364597.4:n.1155+366del
ENST00000487048.5:n.122+366del
NM_012387.2:c.1155+366del NP_036519.2:n.1155+366del
XM_011541150.1:c.969+366del XP_011539452.1:n.969+366del
XM_011541151.1:c.1155+366del XP_011539453.1:n.1155+366del
XM_011541152.1:c.618+366del XP_011539454.1:n.618+366del
XM_011541153.1:c.1156-286del XP_011539455.1:n.1156-286del
XM_011541154.1:c.1156-286del XP_011539456.1:n.1156-286del
XM_011541155.1:c.1155+366del XP_011539457.1:n.1155+366del
XM_011541156.1:c.1155+366del XP_011539458.1:n.1155+366del
XM_011541157.1:c.264+366del XP_011539459.1:n.264+366del
XM_011541154.2:c.1156-286del XP_011539456.1:n.1156-286del
NM_012387.3:c.1155+366del MANE Select NP_036519.2:n.1155+366del