Canonical Allele Identifier: CA1610029770

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529800_10529838delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT , CM000668.2:g.10529800_10529838delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT	GRCh38
NC_000006.11:g.10530033_10530071delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT , CM000668.1:g.10530033_10530071delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT	GRCh37
NC_000006.10:g.10638019_10638057delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT	NCBI36
NG_007469.3:g.42578_42616delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+959_484+997delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000495262.7:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000379597.7:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000397423.6:n.484+959_484+997delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000410107.5:c.67+20642_67+20680delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT	ENSP00000386321.1:n.67+20642_67+20680delinsGACGAACATTTCTGGGTG...
ENST00000474518.1:n.508+959_508+997delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000474983.5:n.1466_1504delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000475577.5:n.254+2140_254+2178delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000483204.1:n.1465_1503delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000485764.1:n.4_40+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000489225.5:n.283+36869_283+36907delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000489819.5:n.175+8206_175+8244delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
ENST00000495262.5:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
NM_145649.4:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_005248999.2:c.658_694+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_006715052.2:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_006715053.2:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_011514465.1:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_011514467.1:c.658_694+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_011514468.1:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XR_926136.1:n.1440_1476+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_006715052.3:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_011514468.3:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XM_017010732.2:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XR_002956275.1:n.1440_1476+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
XR_926136.2:n.1438_1474+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
NM_001374747.1:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT
NM_145649.5:c.889_925+2delinsGACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT