Canonical Allele Identifier: CA478527587

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945736T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793140T>C , CM000674.2:g.7793140T>C	GRCh38
NC_000012.11:g.7945736T>C , CM000674.1:g.7945736T>C	GRCh37
NC_000012.10:g.7837003T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.342T>C MANE Select	ENSP00000229307.4:p.Phe114=
ENST00000229307.8:c.342T>C	ENSP00000229307.4:p.Phe114=
ENST00000526286.1:c.342T>C	ENSP00000435288.1:p.Phe114=
ENST00000526434.2:n.486T>C
ENST00000541267.5:c.270T>C	ENSP00000444434.1:p.Phe90=
NM_001297698.1:c.342T>C	NP_001284627.1:p.Phe114=
NM_024865.3:c.342T>C	NP_079141.2:p.Phe114=
XM_011520850.1:c.342T>C	XP_011519152.1:p.Phe114=
XM_011520851.1:c.270T>C	XP_011519153.1:p.Phe90=
XM_011520852.1:c.-31T>C	XP_011519154.1:n.-31T>C
NM_024865.4:c.342T>C MANE Select	NP_079141.2:p.Phe114=
NM_001297698.2:c.342T>C	NP_001284627.1:p.Phe114=