Canonical Allele Identifier: CA1156099106
Gene: PADI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17117863_17117864delinsAG , CM000663.2:g.17117863_17117864delinsAG GRCh38
NC_000001.10:g.17444358_17444359delinsAG , CM000663.1:g.17444358_17444359delinsAG GRCh37
NC_000001.9:g.17316945_17316946delinsAG NCBI36
NG_033958.1:g.6590_6591delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1416_92+1417delinsCT MANE Select ENSP00000364635.4:n.92+1416_92+1417delinsCT
ENST00000375481.1:c.92+1416_92+1417delinsCT ENSP00000364630.1:n.92+1416_92+1417delinsCT
ENST00000375486.8:c.92+1416_92+1417delinsCT ENSP00000364635.4:n.92+1416_92+1417delinsCT
NM_007365.2:c.92+1416_92+1417delinsCT NP_031391.2:n.92+1416_92+1417delinsCT
XM_011540549.1:c.92+1416_92+1417delinsCT XP_011538851.1:n.92+1416_92+1417delinsCT
XR_947004.1:n.4439_4440delinsAG
XR_001736944.1:n.174+1416_174+1417delinsCT
NM_007365.3:c.92+1416_92+1417delinsCT MANE Select NP_031391.2:n.92+1416_92+1417delinsCT