Canonical Allele Identifier: CA1610029981

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529883_10529887delinsGTCAA , CM000668.2:g.10529883_10529887delinsGTCAA	GRCh38
NC_000006.11:g.10530116_10530120delinsGTCAA , CM000668.1:g.10530116_10530120delinsGTCAA	GRCh37
NC_000006.10:g.10638102_10638106delinsGTCAA	NCBI36
NG_007469.3:g.42661_42665delinsGTCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+1042_484+1046delinsGTCAA
ENST00000495262.7:c.925+47_925+51delinsGTCAA MANE Select	ENSP00000419411.2:n.925+47_925+51delinsGTCAA
ENST00000379597.7:c.925+47_925+51delinsGTCAA	ENSP00000368917.3:n.925+47_925+51delinsGTCAA
ENST00000397423.6:n.484+1042_484+1046delinsGTCAA
ENST00000410107.5:c.67+20725_67+20729delinsGTCAA	ENSP00000386321.1:n.67+20725_67+20729delinsGTCAA
ENST00000461400.1:n.25+47_25+51delinsGTCAA
ENST00000474518.1:n.508+1042_508+1046delinsGTCAA
ENST00000474983.5:n.1549_1553delinsGTCAA
ENST00000475577.5:n.254+2223_254+2227delinsGTCAA
ENST00000483204.1:n.1548_1552delinsGTCAA
ENST00000485764.1:n.40+47_40+51delinsGTCAA
ENST00000489225.5:n.283+36952_283+36956delinsGTCAA
ENST00000489819.5:n.175+8289_175+8293delinsGTCAA
ENST00000495262.5:c.925+47_925+51delinsGTCAA	ENSP00000419411.1:n.925+47_925+51delinsGTCAA
NM_145649.4:c.925+47_925+51delinsGTCAA	NP_663624.1:n.925+47_925+51delinsGTCAA
XM_005248999.2:c.694+47_694+51delinsGTCAA	XP_005249056.1:n.694+47_694+51delinsGTCAA
XM_006715052.2:c.925+47_925+51delinsGTCAA	XP_006715115.1:n.925+47_925+51delinsGTCAA
XM_006715053.2:c.925+47_925+51delinsGTCAA	XP_006715116.1:n.925+47_925+51delinsGTCAA
XM_011514465.1:c.925+47_925+51delinsGTCAA	XP_011512767.1:n.925+47_925+51delinsGTCAA
XM_011514467.1:c.694+47_694+51delinsGTCAA	XP_011512769.1:n.694+47_694+51delinsGTCAA
XM_011514468.1:c.925+47_925+51delinsGTCAA	XP_011512770.1:n.925+47_925+51delinsGTCAA
XR_926136.1:n.1476+47_1476+51delinsGTCAA
XM_006715052.3:c.925+47_925+51delinsGTCAA	XP_006715115.1:n.925+47_925+51delinsGTCAA
XM_011514468.3:c.925+47_925+51delinsGTCAA	XP_011512770.1:n.925+47_925+51delinsGTCAA
XM_017010732.2:c.925+47_925+51delinsGTCAA	XP_016866221.1:n.925+47_925+51delinsGTCAA
XR_002956275.1:n.1476+47_1476+51delinsGTCAA
XR_926136.2:n.1474+47_1474+51delinsGTCAA
NM_001374747.1:c.925+47_925+51delinsGTCAA	NP_001361676.1:n.925+47_925+51delinsGTCAA
NM_145649.5:c.925+47_925+51delinsGTCAA MANE Select	NP_663624.1:n.925+47_925+51delinsGTCAA