Canonical Allele Identifier: CA15928462
Gene: NAPG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10535063T>A , CM000680.2:g.10535063T>A GRCh38
NC_000018.9:g.10535060T>A , CM000680.1:g.10535060T>A GRCh37
NC_000018.8:g.10525060T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000322897.11:c.258+567T>A MANE Select ENSP00000324628.6:n.258+567T>A
ENST00000322897.10:c.258+567T>A ENSP00000324628.6:n.258+567T>A
ENST00000580224.5:c.*121+567T>A ENSP00000463265.1:n.*121+567T>A
ENST00000580483.5:c.57-4699T>A ENSP00000464496.1:n.57-4699T>A
ENST00000582472.3:c.393+567T>A ENSP00000463018.3:n.393+567T>A
ENST00000582978.5:n.259+567T>A
NM_003826.2:c.258+567T>A NP_003817.1:n.258+567T>A
XM_011525754.1:c.438+567T>A XP_011524056.1:n.438+567T>A
XM_011525755.1:c.303+567T>A XP_011524057.1:n.303+567T>A
XM_011525756.1:c.12+567T>A XP_011524058.1:n.12+567T>A
XM_011525754.2:c.438+567T>A XP_011524056.1:n.438+567T>A
XM_011525756.2:c.12+567T>A XP_011524058.1:n.12+567T>A
NM_003826.3:c.258+567T>A MANE Select NP_003817.1:n.258+567T>A
Search 100 bp 5'
Search 100 bp 3'