Canonical Allele Identifier: CA2014710195
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1862859151

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792736_7792740del , CM000674.2:g.7792736_7792740del GRCh38
NC_000012.11:g.7945332_7945336del , CM000674.1:g.7945332_7945336del GRCh37
NC_000012.10:g.7836599_7836603del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-214_152-210del MANE Select ENSP00000229307.4:n.152-214_152-210del
ENST00000229307.8:c.152-214_152-210del ENSP00000229307.4:n.152-214_152-210del
ENST00000526286.1:c.152-214_152-210del ENSP00000435288.1:n.152-214_152-210del
ENST00000526434.2:n.334-252_334-248del
ENST00000541267.5:c.80-214_80-210del ENSP00000444434.1:n.80-214_80-210del
NM_001297698.1:c.152-214_152-210del NP_001284627.1:n.152-214_152-210del
NM_024865.3:c.152-214_152-210del NP_079141.2:n.152-214_152-210del
XM_011520850.1:c.152-214_152-210del XP_011519152.1:n.152-214_152-210del
XM_011520851.1:c.80-214_80-210del XP_011519153.1:n.80-214_80-210del
XM_011520852.1:c.-183-252_-183-248del XP_011519154.1:n.-183-252_-183-248del
NM_024865.4:c.152-214_152-210del MANE Select NP_079141.2:n.152-214_152-210del
NM_001297698.2:c.152-214_152-210del NP_001284627.1:n.152-214_152-210del