Canonical Allele Identifier: CA1139915339
Gene: PADI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118157G= , CM000663.2:g.17118157G= GRCh38
NC_000001.10:g.17444652G= , CM000663.1:g.17444652G= GRCh37
NC_000001.9:g.17317239G= NCBI36
NG_033958.1:g.6297C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1123C= MANE Select ENSP00000364635.4:n.92+1123C=
ENST00000375481.1:c.92+1123C= ENSP00000364630.1:n.92+1123C=
ENST00000375486.8:c.92+1123C= ENSP00000364635.4:n.92+1123C=
NM_007365.2:c.92+1123C= NP_031391.2:n.92+1123C=
XM_011540549.1:c.92+1123C= XP_011538851.1:n.92+1123C=
XR_947004.1:n.4733G=
XR_001736944.1:n.174+1123C=
NM_007365.3:c.92+1123C= MANE Select NP_031391.2:n.92+1123C=