Canonical Allele Identifier: CA2843610221
Gene: PADI4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17336049_17336050insA , CM000663.2:g.17336049_17336050insA GRCh38
NC_000001.10:g.17662544_17662545insA , CM000663.1:g.17662544_17662545insA GRCh37
NC_000001.9:g.17535131_17535132insA NCBI36
NG_023261.2:g.32860_32861insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375448.4:c.341-110_341-109insA MANE Select ENSP00000364597.4:n.341-110_341-109insA
NM_012387.2:c.341-110_341-109insA NP_036519.2:n.341-110_341-109insA
XM_011541150.1:c.340+2040_340+2041insA XP_011539452.1:n.340+2040_340+2041insA
XM_011541151.1:c.341-110_341-109insA XP_011539453.1:n.341-110_341-109insA
XM_011541152.1:c.-79-110_-79-109insA XP_011539454.1:n.-79-110_-79-109insA
XM_011541153.1:c.341-110_341-109insA XP_011539455.1:n.341-110_341-109insA
XM_011541154.1:c.341-110_341-109insA XP_011539456.1:n.341-110_341-109insA
XM_011541155.1:c.341-110_341-109insA XP_011539457.1:n.341-110_341-109insA
XM_011541156.1:c.341-110_341-109insA XP_011539458.1:n.341-110_341-109insA
XM_011541157.1:c.-372-110_-372-109insA XP_011539459.1:n.-372-110_-372-109insA
XM_011541154.2:c.341-110_341-109insA XP_011539456.1:n.341-110_341-109insA
NM_012387.3:c.341-110_341-109insA MANE Select NP_036519.2:n.341-110_341-109insA