Canonical Allele Identifier: CA2014710194
Gene: NANOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792734_7792739delinsGTCTAT , CM000674.2:g.7792734_7792739delinsGTCTAT GRCh38
NC_000012.11:g.7945330_7945335delinsGTCTAT , CM000674.1:g.7945330_7945335delinsGTCTAT GRCh37
NC_000012.10:g.7836597_7836602delinsGTCTAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-216_152-211delinsGTCTAT MANE Select ENSP00000229307.4:n.152-216_152-211delins...
ENST00000229307.8:c.152-216_152-211delinsGTCTAT ENSP00000229307.4:n.152-216_152-211delins...
ENST00000526286.1:c.152-216_152-211delinsGTCTAT ENSP00000435288.1:n.152-216_152-211delins...
ENST00000526434.2:n.334-254_334-249delinsGTCTAT
ENST00000541267.5:c.80-216_80-211delinsGTCTAT ENSP00000444434.1:n.80-216_80-211delinsGT...
NM_001297698.1:c.152-216_152-211delinsGTCTAT NP_001284627.1:n.152-216_152-211delinsGTC...
NM_024865.3:c.152-216_152-211delinsGTCTAT NP_079141.2:n.152-216_152-211delinsGTCTAT...
XM_011520850.1:c.152-216_152-211delinsGTCTAT XP_011519152.1:n.152-216_152-211delinsGTC...
XM_011520851.1:c.80-216_80-211delinsGTCTAT XP_011519153.1:n.80-216_80-211delinsGTCTA...
XM_011520852.1:c.-183-254_-183-249delinsGTCTAT XP_011519154.1:n.-183-254_-183-249delinsG...
NM_024865.4:c.152-216_152-211delinsGTCTAT MANE Select NP_079141.2:n.152-216_152-211delinsGTCTAT...
NM_001297698.2:c.152-216_152-211delinsGTCTAT NP_001284627.1:n.152-216_152-211delinsGTC...