Canonical Allele Identifier: CA1156200647
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348413_17348414delinsAT , CM000663.2:g.17348413_17348414delinsAT GRCh38
NC_000001.10:g.17674908_17674909delinsAT , CM000663.1:g.17674908_17674909delinsAT GRCh37
NC_000001.9:g.17547495_17547496delinsAT NCBI36
NG_023261.2:g.45224_45225delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+365_1155+366delinsAT MANE Select ENSP00000364597.4:n.1155+365_1155+366delinsAT
ENST00000487048.5:n.122+365_122+366delinsAT
NM_012387.2:c.1155+365_1155+366delinsAT NP_036519.2:n.1155+365_1155+366delinsAT
XM_011541150.1:c.969+365_969+366delinsAT XP_011539452.1:n.969+365_969+366delinsAT
XM_011541151.1:c.1155+365_1155+366delinsAT XP_011539453.1:n.1155+365_1155+366delinsAT
XM_011541152.1:c.618+365_618+366delinsAT XP_011539454.1:n.618+365_618+366delinsAT
XM_011541153.1:c.1156-287_1156-286delinsAT XP_011539455.1:n.1156-287_1156-286delinsAT
XM_011541154.1:c.1156-287_1156-286delinsAT XP_011539456.1:n.1156-287_1156-286delinsAT
XM_011541155.1:c.1155+365_1155+366delinsAT XP_011539457.1:n.1155+365_1155+366delinsAT
XM_011541156.1:c.1155+365_1155+366delinsAT XP_011539458.1:n.1155+365_1155+366delinsAT
XM_011541157.1:c.264+365_264+366delinsAT XP_011539459.1:n.264+365_264+366delinsAT
XM_011541154.2:c.1156-287_1156-286delinsAT XP_011539456.1:n.1156-287_1156-286delinsAT
NM_012387.3:c.1155+365_1155+366delinsAT MANE Select NP_036519.2:n.1155+365_1155+366delinsAT