Canonical Allele Identifier: CA2284348496

Gene: NAPG

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10549365C>T , CM000680.2:g.10549365C>T	GRCh38
NC_000018.9:g.10549362C>T , CM000680.1:g.10549362C>T	GRCh37
NC_000018.8:g.10539362C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322897.11:c.795+269C>T MANE Select	ENSP00000324628.6:n.795+269C>T
ENST00000322897.10:c.795+269C>T	ENSP00000324628.6:n.795+269C>T
ENST00000580224.5:c.*658+269C>T	ENSP00000463265.1:n.*658+269C>T
ENST00000580483.5:c.*536+269C>T	ENSP00000464496.1:n.*536+269C>T
ENST00000583367.1:n.1175+269C>T
NM_003826.2:c.795+269C>T	NP_003817.1:n.795+269C>T
XM_011525754.1:c.975+269C>T	XP_011524056.1:n.975+269C>T
XM_011525755.1:c.840+269C>T	XP_011524057.1:n.840+269C>T
XM_011525756.1:c.549+269C>T	XP_011524058.1:n.549+269C>T
XM_011525754.2:c.975+269C>T	XP_011524056.1:n.975+269C>T
XM_011525756.2:c.549+269C>T	XP_011524058.1:n.549+269C>T
XM_017026063.2:c.540+269C>T	XP_016881552.1:n.540+269C>T
NM_003826.3:c.795+269C>T MANE Select	NP_003817.1:n.795+269C>T