Canonical Allele Identifier: CA383781190

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945769G>T (hg19) ; chr12:g.7793173G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793173G>T , CM000674.2:g.7793173G>T	GRCh38
NC_000012.11:g.7945769G>T , CM000674.1:g.7945769G>T	GRCh37
NC_000012.10:g.7837036G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.375G>T MANE Select	ENSP00000229307.4:p.Met125Ile
ENST00000229307.8:c.375G>T	ENSP00000229307.4:p.Met125Ile
ENST00000526286.1:c.375G>T	ENSP00000435288.1:p.Met125Ile
ENST00000526434.2:n.519G>T
ENST00000541267.5:c.303G>T	ENSP00000444434.1:p.Met101Ile
NM_001297698.1:c.375G>T	NP_001284627.1:p.Met125Ile
NM_024865.3:c.375G>T	NP_079141.2:p.Met125Ile
XM_011520850.1:c.375G>T	XP_011519152.1:p.Met125Ile
XM_011520851.1:c.303G>T	XP_011519153.1:p.Met101Ile
XM_011520852.1:c.3G>T	XP_011519154.1:p.Met1Ile
NM_024865.4:c.375G>T MANE Select	NP_079141.2:p.Met125Ile
NM_001297698.2:c.375G>T	NP_001284627.1:p.Met125Ile