Canonical Allele Identifier: CA2725250725

Gene: NANOG

Linked Data

• dbSNP Id: rs142208324

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792829_7792831dup , CM000674.2:g.7792829_7792831dup	GRCh38
NC_000012.11:g.7945425_7945427dup , CM000674.1:g.7945425_7945427dup	GRCh37
NC_000012.10:g.7836692_7836694dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000229307.9:c.152-121_152-119dup MANE Select	ENSP00000229307.4:n.152-121_152-119dup
ENST00000229307.8:c.152-121_152-119dup	ENSP00000229307.4:n.152-121_152-119dup
ENST00000526286.1:c.152-121_152-119dup	ENSP00000435288.1:n.152-121_152-119dup
ENST00000526434.2:n.334-159_334-157dup
ENST00000541267.5:c.80-121_80-119dup	ENSP00000444434.1:n.80-121_80-119dup
NM_001297698.1:c.152-121_152-119dup	NP_001284627.1:n.152-121_152-119dup
NM_024865.3:c.152-121_152-119dup	NP_079141.2:n.152-121_152-119dup
XM_011520850.1:c.152-121_152-119dup	XP_011519152.1:n.152-121_152-119dup
XM_011520851.1:c.80-121_80-119dup	XP_011519153.1:n.80-121_80-119dup
XM_011520852.1:c.-183-159_-183-157dup	XP_011519154.1:n.-183-159_-183-157dup
NM_024865.4:c.152-121_152-119dup MANE Select	NP_079141.2:n.152-121_152-119dup
NM_001297698.2:c.152-121_152-119dup	NP_001284627.1:n.152-121_152-119dup