Canonical Allele Identifier: CA2501315949

Gene: NANOG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792868_7792869insATAAGAAG , CM000674.2:g.7792868_7792869insATAAGAAG	GRCh38
NC_000012.11:g.7945464_7945465insATAAGAAG , CM000674.1:g.7945464_7945465insATAAGAAG	GRCh37
NC_000012.10:g.7836731_7836732insATAAGAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-82_152-81insATAAGAAG MANE Select	ENSP00000229307.4:n.152-82_152-81insATAAGAAG
ENST00000229307.8:c.152-82_152-81insATAAGAAG	ENSP00000229307.4:n.152-82_152-81insATAAGAAG
ENST00000526286.1:c.152-82_152-81insATAAGAAG	ENSP00000435288.1:n.152-82_152-81insATAAGAAG
ENST00000526434.2:n.334-120_334-119insATAAGAAG
ENST00000541267.5:c.80-82_80-81insATAAGAAG	ENSP00000444434.1:n.80-82_80-81insATAAGAAG
NM_001297698.1:c.152-82_152-81insATAAGAAG	NP_001284627.1:n.152-82_152-81insATAAGAAG
NM_024865.3:c.152-82_152-81insATAAGAAG	NP_079141.2:n.152-82_152-81insATAAGAAG
XM_011520850.1:c.152-82_152-81insATAAGAAG	XP_011519152.1:n.152-82_152-81insATAAGAAG
XM_011520851.1:c.80-82_80-81insATAAGAAG	XP_011519153.1:n.80-82_80-81insATAAGAAG
XM_011520852.1:c.-183-120_-183-119insATAAGAAG	XP_011519154.1:n.-183-120_-183-119insATAAGAAG
NM_024865.4:c.152-82_152-81insATAAGAAG MANE Select	NP_079141.2:n.152-82_152-81insATAAGAAG
NM_001297698.2:c.152-82_152-81insATAAGAAG	NP_001284627.1:n.152-82_152-81insATAAGAAG