Canonical Allele Identifier: CA1156187341
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336345_17336346delinsGA , CM000663.2:g.17336345_17336346delinsGA GRCh38
NC_000001.10:g.17662840_17662841delinsGA , CM000663.1:g.17662840_17662841delinsGA GRCh37
NC_000001.9:g.17535427_17535428delinsGA NCBI36
NG_023261.2:g.33156_33157delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.408+119_408+120delinsGA MANE Select ENSP00000364597.4:n.408+119_408+120delinsGA
NM_012387.2:c.408+119_408+120delinsGA NP_036519.2:n.408+119_408+120delinsGA
XM_011541150.1:c.340+2336_340+2337delinsGA XP_011539452.1:n.340+2336_340+2337delinsGA
XM_011541151.1:c.408+119_408+120delinsGA XP_011539453.1:n.408+119_408+120delinsGA
XM_011541152.1:c.-12+119_-12+120delinsGA XP_011539454.1:n.-12+119_-12+120delinsGA
XM_011541153.1:c.408+119_408+120delinsGA XP_011539455.1:n.408+119_408+120delinsGA
XM_011541154.1:c.408+119_408+120delinsGA XP_011539456.1:n.408+119_408+120delinsGA
XM_011541155.1:c.408+119_408+120delinsGA XP_011539457.1:n.408+119_408+120delinsGA
XM_011541156.1:c.408+119_408+120delinsGA XP_011539458.1:n.408+119_408+120delinsGA
XM_011541157.1:c.-305+119_-305+120delinsGA XP_011539459.1:n.-305+119_-305+120delinsGA
XM_011541154.2:c.408+119_408+120delinsGA XP_011539456.1:n.408+119_408+120delinsGA
NM_012387.3:c.408+119_408+120delinsGA MANE Select NP_036519.2:n.408+119_408+120delinsGA