Canonical Allele Identifier: CA1610029896

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529849_10529851delinsCTT , CM000668.2:g.10529849_10529851delinsCTT	GRCh38
NC_000006.11:g.10530082_10530084delinsCTT , CM000668.1:g.10530082_10530084delinsCTT	GRCh37
NC_000006.10:g.10638068_10638070delinsCTT	NCBI36
NG_007469.3:g.42627_42629delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+1008_484+1010delinsCTT
ENST00000495262.7:c.925+13_925+15delinsCTT MANE Select	ENSP00000419411.2:n.925+13_925+15delinsCTT
ENST00000379597.7:c.925+13_925+15delinsCTT	ENSP00000368917.3:n.925+13_925+15delinsCTT
ENST00000397423.6:n.484+1008_484+1010delinsCTT
ENST00000410107.5:c.67+20691_67+20693delinsCTT	ENSP00000386321.1:n.67+20691_67+20693delinsCTT
ENST00000461400.1:n.25+13_25+15delinsCTT
ENST00000474518.1:n.508+1008_508+1010delinsCTT
ENST00000474983.5:n.1515_1517delinsCTT
ENST00000475577.5:n.254+2189_254+2191delinsCTT
ENST00000483204.1:n.1514_1516delinsCTT
ENST00000485764.1:n.40+13_40+15delinsCTT
ENST00000489225.5:n.283+36918_283+36920delinsCTT
ENST00000489819.5:n.175+8255_175+8257delinsCTT
ENST00000495262.5:c.925+13_925+15delinsCTT	ENSP00000419411.1:n.925+13_925+15delinsCTT
NM_145649.4:c.925+13_925+15delinsCTT	NP_663624.1:n.925+13_925+15delinsCTT
XM_005248999.2:c.694+13_694+15delinsCTT	XP_005249056.1:n.694+13_694+15delinsCTT
XM_006715052.2:c.925+13_925+15delinsCTT	XP_006715115.1:n.925+13_925+15delinsCTT
XM_006715053.2:c.925+13_925+15delinsCTT	XP_006715116.1:n.925+13_925+15delinsCTT
XM_011514465.1:c.925+13_925+15delinsCTT	XP_011512767.1:n.925+13_925+15delinsCTT
XM_011514467.1:c.694+13_694+15delinsCTT	XP_011512769.1:n.694+13_694+15delinsCTT
XM_011514468.1:c.925+13_925+15delinsCTT	XP_011512770.1:n.925+13_925+15delinsCTT
XR_926136.1:n.1476+13_1476+15delinsCTT
XM_006715052.3:c.925+13_925+15delinsCTT	XP_006715115.1:n.925+13_925+15delinsCTT
XM_011514468.3:c.925+13_925+15delinsCTT	XP_011512770.1:n.925+13_925+15delinsCTT
XM_017010732.2:c.925+13_925+15delinsCTT	XP_016866221.1:n.925+13_925+15delinsCTT
XR_002956275.1:n.1476+13_1476+15delinsCTT
XR_926136.2:n.1474+13_1474+15delinsCTT
NM_001374747.1:c.925+13_925+15delinsCTT	NP_001361676.1:n.925+13_925+15delinsCTT
NM_145649.5:c.925+13_925+15delinsCTT MANE Select	NP_663624.1:n.925+13_925+15delinsCTT