Canonical Allele Identifier: CA1156099489
Gene: PADI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118260C= , CM000663.2:g.17118260C= GRCh38
NC_000001.10:g.17444755C= , CM000663.1:g.17444755C= GRCh37
NC_000001.9:g.17317342C= NCBI36
NG_033958.1:g.6194G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375486.9:c.92+1020G= MANE Select ENSP00000364635.4:n.92+1020G=
ENST00000375481.1:c.92+1020G= ENSP00000364630.1:n.92+1020G=
ENST00000375486.8:c.92+1020G= ENSP00000364635.4:n.92+1020G=
NM_007365.2:c.92+1020G= NP_031391.2:n.92+1020G=
XM_011540549.1:c.92+1020G= XP_011538851.1:n.92+1020G=
XR_947004.1:n.4836C=
XR_001736944.1:n.174+1020G=
NM_007365.3:c.92+1020G= MANE Select NP_031391.2:n.92+1020G=
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