Canonical Allele Identifier: CA2014710555

Gene: NANOG

Linked Data

• dbSNP Id: rs1862864885

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793070dup , CM000674.2:g.7793070dup	GRCh38
NC_000012.11:g.7945666dup , CM000674.1:g.7945666dup	GRCh37
NC_000012.10:g.7836933dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.272dup MANE Select	ENSP00000229307.4:p.Val93GlyfsTer20
ENST00000229307.8:c.272dup	ENSP00000229307.4:p.Val93GlyfsTer20
ENST00000526286.1:c.272dup	ENSP00000435288.1:p.Val93GlyfsTer20
ENST00000526434.2:n.416dup
ENST00000541267.5:c.200dup	ENSP00000444434.1:p.Val69GlyfsTer20
NM_001297698.1:c.272dup	NP_001284627.1:p.Val93GlyfsTer20
NM_024865.3:c.272dup	NP_079141.2:p.Val93GlyfsTer20
XM_011520850.1:c.272dup	XP_011519152.1:p.Val93GlyfsTer20
XM_011520851.1:c.200dup	XP_011519153.1:p.Val69GlyfsTer20
XM_011520852.1:c.-101dup	XP_011519154.1:n.-101dup
NM_024865.4:c.272dup MANE Select	NP_079141.2:p.Val93GlyfsTer20
NM_001297698.2:c.272dup	NP_001284627.1:p.Val93GlyfsTer20