Canonical Allele Identifier: CA478527613

Gene: NANOG

Linked Data

• gnomAD v4: 12-7793191-C-T
• MyVariant Identifiers: chr12:g.7945787C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793191C>T , CM000674.2:g.7793191C>T	GRCh38
NC_000012.11:g.7945787C>T , CM000674.1:g.7945787C>T	GRCh37
NC_000012.10:g.7837054C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.393C>T MANE Select	ENSP00000229307.4:p.Ile131=
ENST00000229307.8:c.393C>T	ENSP00000229307.4:p.Ile131=
ENST00000526286.1:c.393C>T	ENSP00000435288.1:p.Ile131=
ENST00000526434.2:n.537C>T
ENST00000541267.5:c.321C>T	ENSP00000444434.1:p.Ile107=
NM_001297698.1:c.393C>T	NP_001284627.1:p.Ile131=
NM_024865.3:c.393C>T	NP_079141.2:p.Ile131=
XM_011520850.1:c.393C>T	XP_011519152.1:p.Ile131=
XM_011520851.1:c.321C>T	XP_011519153.1:p.Ile107=
XM_011520852.1:c.21C>T	XP_011519154.1:p.Ile7=
NM_024865.4:c.393C>T MANE Select	NP_079141.2:p.Ile131=
NM_001297698.2:c.393C>T	NP_001284627.1:p.Ile131=