Canonical Allele Identifier: CA383780606

Gene: NANOG

Linked Data

• MyVariant Identifiers: chr12:g.7945666T>C (hg19) ; chr12:g.7793070T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.272T>C MANE Select	ENSP00000229307.4:p.Val91Ala
ENST00000229307.8:c.272T>C	ENSP00000229307.4:p.Val91Ala
ENST00000526286.1:c.272T>C	ENSP00000435288.1:p.Val91Ala
ENST00000526434.2:n.416T>C
ENST00000541267.5:c.200T>C	ENSP00000444434.1:p.Val67Ala
NM_001297698.1:c.272T>C	NP_001284627.1:p.Val91Ala
NM_024865.3:c.272T>C	NP_079141.2:p.Val91Ala
XM_011520850.1:c.272T>C	XP_011519152.1:p.Val91Ala
XM_011520851.1:c.200T>C	XP_011519153.1:p.Val67Ala
XM_011520852.1:c.-101T>C	XP_011519154.1:n.-101T>C
NM_024865.4:c.272T>C MANE Select	NP_079141.2:p.Val91Ala
NM_001297698.2:c.272T>C	NP_001284627.1:p.Val91Ala