Canonical Allele Identifier: CA10625352

Gene: GCNT2

Linked Data

• ClinVar Variation Id: 354692
• ClinVar RCV Id: RCV000387849
• dbSNP Id: rs886060900
• MyVariant Identifiers: chr6:g.10555995_10556000delinsCCCCACTTTTT (hg19) ; chr6:g.10555762_10555767delinsCCCCACTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10555762_10555767delinsCCCCACTTTTT , CM000668.2:g.10555762_10555767delinsCCCCACTTTTT	GRCh38
NC_000006.11:g.10555995_10556000delinsCCCCACTTTTT , CM000668.1:g.10555995_10556000delinsCCCCACTTTTT	GRCh37
NC_000006.10:g.10663981_10663986delinsCCCCACTTTTT	NCBI36
NG_007469.3:g.68540_68545delinsCCCCACTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000397423.7:n.484+26921_484+26926delinsCCCCACTTTTT
ENST00000495262.7:c.925+25926_925+25931delinsCCCCACTTTTT MANE Select	ENSP00000419411.2:n.925+25926_925+25931delinsCCCCACTTTTT
ENST00000379597.7:c.925+25926_925+25931delinsCCCCACTTTTT	ENSP00000368917.3:n.925+25926_925+25931delinsCCCCACTTTTT
ENST00000397423.6:n.484+26921_484+26926delinsCCCCACTTTTT
ENST00000410107.5:c.67+46604_67+46609delinsCCCCACTTTTT	ENSP00000386321.1:n.67+46604_67+46609delinsCCCCACTTTTT
ENST00000461400.1:n.25+25926_25+25931delinsCCCCACTTTTT
ENST00000474518.1:n.508+26921_508+26926delinsCCCCACTTTTT
ENST00000475577.5:n.254+28102_254+28107delinsCCCCACTTTTT
ENST00000485764.1:n.40+25926_40+25931delinsCCCCACTTTTT
ENST00000489225.5:n.283+62831_283+62836delinsCCCCACTTTTT
ENST00000489819.5:n.175+34168_175+34173delinsCCCCACTTTTT
ENST00000495262.5:c.925+25926_925+25931delinsCCCCACTTTTT	ENSP00000419411.1:n.925+25926_925+25931delinsCCCCACTTTTT
NM_001491.2:c.-662_-657delinsCCCCACTTTTT	NP_001482.1:n.-662_-657delinsCCCCACTTTTT
NM_145649.4:c.925+25926_925+25931delinsCCCCACTTTTT	NP_663624.1:n.925+25926_925+25931delinsCCCCACTTTTT
XM_005248999.2:c.694+25926_694+25931delinsCCCCACTTTTT	XP_005249056.1:n.694+25926_694+25931delinsCCCCACTTTTT
XM_006715052.2:c.925+25926_925+25931delinsCCCCACTTTTT	XP_006715115.1:n.925+25926_925+25931delinsCCCCACTTTTT
XM_006715053.2:c.926-72_926-67delinsCCCCACTTTTT	XP_006715116.1:n.926-72_926-67delinsCCCCACTTTTT
XM_011514465.1:c.926-17368_926-17363delinsCCCCACTTTTT	XP_011512767.1:n.926-17368_926-17363delinsCCCCACTTTTT
XM_011514467.1:c.694+25926_694+25931delinsCCCCACTTTTT	XP_011512769.1:n.694+25926_694+25931delinsCCCCACTTTTT
XR_926136.1:n.1476+25926_1476+25931delinsCCCCACTTTTT
XM_006715052.3:c.925+25926_925+25931delinsCCCCACTTTTT	XP_006715115.1:n.925+25926_925+25931delinsCCCCACTTTTT
XR_002956275.1:n.1476+25926_1476+25931delinsCCCCACTTTTT
XR_926136.2:n.1474+25926_1474+25931delinsCCCCACTTTTT
NM_001374747.1:c.925+25926_925+25931delinsCCCCACTTTTT	NP_001361676.1:n.925+25926_925+25931delinsCCCCACTTTTT
NM_145649.5:c.925+25926_925+25931delinsCCCCACTTTTT MANE Select	NP_663624.1:n.925+25926_925+25931delinsCCCCACTTTTT