Canonical Allele Identifier: CA1156099332
Gene: PADI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118092T= , CM000663.2:g.17118092T= GRCh38
NC_000001.10:g.17444587T= , CM000663.1:g.17444587T= GRCh37
NC_000001.9:g.17317174T= NCBI36
NG_033958.1:g.6362A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1188A= MANE Select ENSP00000364635.4:n.92+1188A=
ENST00000375481.1:c.92+1188A= ENSP00000364630.1:n.92+1188A=
ENST00000375486.8:c.92+1188A= ENSP00000364635.4:n.92+1188A=
NM_007365.2:c.92+1188A= NP_031391.2:n.92+1188A=
XM_011540549.1:c.92+1188A= XP_011538851.1:n.92+1188A=
XR_947004.1:n.4668T=
XR_001736944.1:n.174+1188A=
NM_007365.3:c.92+1188A= MANE Select NP_031391.2:n.92+1188A=