Canonical Allele Identifier: CA1156099080
Gene: PADI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17117852G= , CM000663.2:g.17117852G= GRCh38
NC_000001.10:g.17444347G= , CM000663.1:g.17444347G= GRCh37
NC_000001.9:g.17316934G= NCBI36
NG_033958.1:g.6602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1428C= MANE Select ENSP00000364635.4:n.92+1428C=
ENST00000375481.1:c.92+1428C= ENSP00000364630.1:n.92+1428C=
ENST00000375486.8:c.92+1428C= ENSP00000364635.4:n.92+1428C=
NM_007365.2:c.92+1428C= NP_031391.2:n.92+1428C=
XM_011540549.1:c.92+1428C= XP_011538851.1:n.92+1428C=
XR_947004.1:n.4428G=
XR_001736944.1:n.174+1428C=
NM_007365.3:c.92+1428C= MANE Select NP_031391.2:n.92+1428C=
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