Canonical Allele Identifier: CA1156099381
Gene: PADI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118134A= , CM000663.2:g.17118134A= GRCh38
NC_000001.10:g.17444629A= , CM000663.1:g.17444629A= GRCh37
NC_000001.9:g.17317216A= NCBI36
NG_033958.1:g.6320T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1146T= MANE Select ENSP00000364635.4:n.92+1146T=
ENST00000375481.1:c.92+1146T= ENSP00000364630.1:n.92+1146T=
ENST00000375486.8:c.92+1146T= ENSP00000364635.4:n.92+1146T=
NM_007365.2:c.92+1146T= NP_031391.2:n.92+1146T=
XM_011540549.1:c.92+1146T= XP_011538851.1:n.92+1146T=
XR_947004.1:n.4710A=
XR_001736944.1:n.174+1146T=
NM_007365.3:c.92+1146T= MANE Select NP_031391.2:n.92+1146T=