Canonical Allele Identifier: CA1156099520
Gene: PADI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118279C= , CM000663.2:g.17118279C= GRCh38
NC_000001.10:g.17444774C= , CM000663.1:g.17444774C= GRCh37
NC_000001.9:g.17317361C= NCBI36
NG_033958.1:g.6175G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1001G= MANE Select ENSP00000364635.4:n.92+1001G=
ENST00000375481.1:c.92+1001G= ENSP00000364630.1:n.92+1001G=
ENST00000375486.8:c.92+1001G= ENSP00000364635.4:n.92+1001G=
NM_007365.2:c.92+1001G= NP_031391.2:n.92+1001G=
XM_011540549.1:c.92+1001G= XP_011538851.1:n.92+1001G=
XR_947004.1:n.4855C=
XR_001736944.1:n.174+1001G=
NM_007365.3:c.92+1001G= MANE Select NP_031391.2:n.92+1001G=
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