Canonical Allele Identifier: CA603489236

Gene: NANOG

Linked Data

• gnomAD v2: 12-7945643-T-TCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
• MyVariant Identifiers: chr12:g.7945643_7945644insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793047_7793048insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA , CM000674.2:g.7793047_7793048insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA	GRCh38
NC_000012.11:g.7945643_7945644insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA , CM000674.1:g.7945643_7945644insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA	GRCh37
NC_000012.10:g.7836910_7836911insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
ENST00000229307.8:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
ENST00000526286.1:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
ENST00000526434.2:n.393_394insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
ENST00000541267.5:c.177_178insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
NM_001297698.1:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
NM_024865.3:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
XM_011520850.1:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
XM_011520851.1:c.177_178insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
XM_011520852.1:c.-124_-123insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA	XP_011519154.1:n.-124_-123insCCATTCTGACCTATTAACACCCAGCGTGGGAG...
NM_024865.4:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA
NM_001297698.2:c.249_250insCCATTCTGACCTATTAACACCCAGCGTGGGAGCTTTTGAGCATCA