Canonical Allele Identifier: CA1112166143

Gene: NUGGC

Linked Data

• dbSNP Id: rs1810433772
• gnomAD v3: 8-28066038-G-GT
• gnomAD v4: 8-28066038-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28066039dup , CM000670.2:g.28066039dup	GRCh38
NC_000008.10:g.27923556dup , CM000670.1:g.27923556dup	GRCh37
NC_000008.9:g.27979475dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413272.7:c.712-1308dup MANE Select	ENSP00000408697.2:n.712-1308dup
ENST00000413272.6:c.712-1308dup	ENSP00000408697.2:n.712-1308dup
NM_001010906.1:c.712-1308dup	NP_001010906.1:n.712-1308dup
XM_011544523.1:c.784-1308dup	XP_011542825.1:n.784-1308dup
XM_011544524.1:c.784-1308dup	XP_011542826.1:n.784-1308dup
XM_011544526.1:c.784-1308dup	XP_011542828.1:n.784-1308dup
XM_011544523.2:c.784-1308dup	XP_011542825.1:n.784-1308dup
XM_011544524.3:c.784-1308dup	XP_011542826.1:n.784-1308dup
XM_011544526.2:c.784-1308dup	XP_011542828.1:n.784-1308dup
XM_017013403.1:c.784-1308dup	XP_016868892.1:n.784-1308dup
NM_001010906.2:c.712-1308dup MANE Select	NP_001010906.1:n.712-1308dup