Canonical Allele Identifier: CA1773116428

Gene: NUGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28065901T= , CM000670.2:g.28065901T=	GRCh38
NC_000008.10:g.27923418T= , CM000670.1:g.27923418T=	GRCh37
NC_000008.9:g.27979337T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000413272.7:c.712-1170A= MANE Select	ENSP00000408697.2:n.712-1170A=
ENST00000413272.6:c.712-1170A=	ENSP00000408697.2:n.712-1170A=
NM_001010906.1:c.712-1170A=	NP_001010906.1:n.712-1170A=
XM_011544523.1:c.784-1170A=	XP_011542825.1:n.784-1170A=
XM_011544524.1:c.784-1170A=	XP_011542826.1:n.784-1170A=
XM_011544526.1:c.784-1170A=	XP_011542828.1:n.784-1170A=
XM_011544523.2:c.784-1170A=	XP_011542825.1:n.784-1170A=
XM_011544524.3:c.784-1170A=	XP_011542826.1:n.784-1170A=
XM_011544526.2:c.784-1170A=	XP_011542828.1:n.784-1170A=
XM_017013403.1:c.784-1170A=	XP_016868892.1:n.784-1170A=
NM_001010906.2:c.712-1170A= MANE Select	NP_001010906.1:n.712-1170A=