Canonical Allele Identifier: CA2617437466

Gene: NANOG

Linked Data

• gnomAD v4: 12-7792800-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792800A>G , CM000674.2:g.7792800A>G	GRCh38
NC_000012.11:g.7945396A>G , CM000674.1:g.7945396A>G	GRCh37
NC_000012.10:g.7836663A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000229307.9:c.152-150A>G MANE Select	ENSP00000229307.4:n.152-150A>G
ENST00000229307.8:c.152-150A>G	ENSP00000229307.4:n.152-150A>G
ENST00000526286.1:c.152-150A>G	ENSP00000435288.1:n.152-150A>G
ENST00000526434.2:n.334-188A>G
ENST00000541267.5:c.80-150A>G	ENSP00000444434.1:n.80-150A>G
NM_001297698.1:c.152-150A>G	NP_001284627.1:n.152-150A>G
NM_024865.3:c.152-150A>G	NP_079141.2:n.152-150A>G
XM_011520850.1:c.152-150A>G	XP_011519152.1:n.152-150A>G
XM_011520851.1:c.80-150A>G	XP_011519153.1:n.80-150A>G
XM_011520852.1:c.-183-188A>G	XP_011519154.1:n.-183-188A>G
NM_024865.4:c.152-150A>G MANE Select	NP_079141.2:n.152-150A>G
NM_001297698.2:c.152-150A>G	NP_001284627.1:n.152-150A>G