Canonical Allele Identifier: CA1773116551

Gene: NUGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28066034A= , CM000670.2:g.28066034A=	GRCh38
NC_000008.10:g.27923551A= , CM000670.1:g.27923551A=	GRCh37
NC_000008.9:g.27979470A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413272.7:c.712-1303T= MANE Select	ENSP00000408697.2:n.712-1303T=
ENST00000413272.6:c.712-1303T=	ENSP00000408697.2:n.712-1303T=
NM_001010906.1:c.712-1303T=	NP_001010906.1:n.712-1303T=
XM_011544523.1:c.784-1303T=	XP_011542825.1:n.784-1303T=
XM_011544524.1:c.784-1303T=	XP_011542826.1:n.784-1303T=
XM_011544526.1:c.784-1303T=	XP_011542828.1:n.784-1303T=
XM_011544523.2:c.784-1303T=	XP_011542825.1:n.784-1303T=
XM_011544524.3:c.784-1303T=	XP_011542826.1:n.784-1303T=
XM_011544526.2:c.784-1303T=	XP_011542828.1:n.784-1303T=
XM_017013403.1:c.784-1303T=	XP_016868892.1:n.784-1303T=
NM_001010906.2:c.712-1303T= MANE Select	NP_001010906.1:n.712-1303T=