Canonical Allele Identifier: CA1156200617
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17348369_17348370delinsCG , CM000663.2:g.17348369_17348370delinsCG GRCh38
NC_000001.10:g.17674864_17674865delinsCG , CM000663.1:g.17674864_17674865delinsCG GRCh37
NC_000001.9:g.17547451_17547452delinsCG NCBI36
NG_023261.2:g.45180_45181delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.1155+321_1155+322delinsCG MANE Select ENSP00000364597.4:n.1155+321_1155+322delinsCG
ENST00000487048.5:n.122+321_122+322delinsCG
NM_012387.2:c.1155+321_1155+322delinsCG NP_036519.2:n.1155+321_1155+322delinsCG
XM_011541150.1:c.969+321_969+322delinsCG XP_011539452.1:n.969+321_969+322delinsCG
XM_011541151.1:c.1155+321_1155+322delinsCG XP_011539453.1:n.1155+321_1155+322delinsCG
XM_011541152.1:c.618+321_618+322delinsCG XP_011539454.1:n.618+321_618+322delinsCG
XM_011541153.1:c.1155+321_1155+322delinsCG XP_011539455.1:n.1155+321_1155+322delinsCG
XM_011541154.1:c.1155+321_1155+322delinsCG XP_011539456.1:n.1155+321_1155+322delinsCG
XM_011541155.1:c.1155+321_1155+322delinsCG XP_011539457.1:n.1155+321_1155+322delinsCG
XM_011541156.1:c.1155+321_1155+322delinsCG XP_011539458.1:n.1155+321_1155+322delinsCG
XM_011541157.1:c.264+321_264+322delinsCG XP_011539459.1:n.264+321_264+322delinsCG
XM_011541154.2:c.1155+321_1155+322delinsCG XP_011539456.1:n.1155+321_1155+322delinsCG
NM_012387.3:c.1155+321_1155+322delinsCG MANE Select NP_036519.2:n.1155+321_1155+322delinsCG