Canonical Allele Identifier: CA1156200471
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348253_17348254delinsAC , CM000663.2:g.17348253_17348254delinsAC GRCh38
NC_000001.10:g.17674748_17674749delinsAC , CM000663.1:g.17674748_17674749delinsAC GRCh37
NC_000001.9:g.17547335_17547336delinsAC NCBI36
NG_023261.2:g.45064_45065delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+205_1155+206delinsAC MANE Select ENSP00000364597.4:n.1155+205_1155+206delinsAC
ENST00000487048.5:n.122+205_122+206delinsAC
NM_012387.2:c.1155+205_1155+206delinsAC NP_036519.2:n.1155+205_1155+206delinsAC
XM_011541150.1:c.969+205_969+206delinsAC XP_011539452.1:n.969+205_969+206delinsAC
XM_011541151.1:c.1155+205_1155+206delinsAC XP_011539453.1:n.1155+205_1155+206delinsAC
XM_011541152.1:c.618+205_618+206delinsAC XP_011539454.1:n.618+205_618+206delinsAC
XM_011541153.1:c.1155+205_1155+206delinsAC XP_011539455.1:n.1155+205_1155+206delinsAC
XM_011541154.1:c.1155+205_1155+206delinsAC XP_011539456.1:n.1155+205_1155+206delinsAC
XM_011541155.1:c.1155+205_1155+206delinsAC XP_011539457.1:n.1155+205_1155+206delinsAC
XM_011541156.1:c.1155+205_1155+206delinsAC XP_011539458.1:n.1155+205_1155+206delinsAC
XM_011541157.1:c.264+205_264+206delinsAC XP_011539459.1:n.264+205_264+206delinsAC
XM_011541154.2:c.1155+205_1155+206delinsAC XP_011539456.1:n.1155+205_1155+206delinsAC
NM_012387.3:c.1155+205_1155+206delinsAC MANE Select NP_036519.2:n.1155+205_1155+206delinsAC