Canonical Allele Identifier: CA1156099111
Gene: PADI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17117873T= , CM000663.2:g.17117873T= GRCh38
NC_000001.10:g.17444368T= , CM000663.1:g.17444368T= GRCh37
NC_000001.9:g.17316955T= NCBI36
NG_033958.1:g.6581A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1407A= MANE Select ENSP00000364635.4:n.92+1407A=
ENST00000375481.1:c.92+1407A= ENSP00000364630.1:n.92+1407A=
ENST00000375486.8:c.92+1407A= ENSP00000364635.4:n.92+1407A=
NM_007365.2:c.92+1407A= NP_031391.2:n.92+1407A=
XM_011540549.1:c.92+1407A= XP_011538851.1:n.92+1407A=
XR_947004.1:n.4449T=
XR_001736944.1:n.174+1407A=
NM_007365.3:c.92+1407A= MANE Select NP_031391.2:n.92+1407A=
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