Canonical Allele Identifier: CA603171030

Gene: NANOG

Linked Data

• dbSNP Id: rs1177273216
• gnomAD v2: 12-7945262-ATTT-A
• gnomAD v3: 12-7792666-ATTT-A
• gnomAD v4: 12-7792666-ATTT-A
• MyVariant Identifiers: chr12:g.7945263_7945265del (hg19) ; chr12:g.7792667_7792669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7792668_7792670del , CM000674.2:g.7792668_7792670del	GRCh38
NC_000012.11:g.7945264_7945266del , CM000674.1:g.7945264_7945266del	GRCh37
NC_000012.10:g.7836531_7836533del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.152-282_152-280del MANE Select	ENSP00000229307.4:n.152-282_152-280del
ENST00000229307.8:c.152-282_152-280del	ENSP00000229307.4:n.152-282_152-280del
ENST00000526286.1:c.152-282_152-280del	ENSP00000435288.1:n.152-282_152-280del
ENST00000526434.2:n.334-320_334-318del
ENST00000541267.5:c.80-282_80-280del	ENSP00000444434.1:n.80-282_80-280del
NM_001297698.1:c.152-282_152-280del	NP_001284627.1:n.152-282_152-280del
NM_024865.3:c.152-282_152-280del	NP_079141.2:n.152-282_152-280del
XM_011520850.1:c.152-282_152-280del	XP_011519152.1:n.152-282_152-280del
XM_011520851.1:c.80-282_80-280del	XP_011519153.1:n.80-282_80-280del
XM_011520852.1:c.-183-320_-183-318del	XP_011519154.1:n.-183-320_-183-318del
NM_024865.4:c.152-282_152-280del MANE Select	NP_079141.2:n.152-282_152-280del
NM_001297698.2:c.152-282_152-280del	NP_001284627.1:n.152-282_152-280del