Canonical Allele Identifier: CA1610027700

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556061_10556065delinsTGAAA , CM000668.2:g.10556061_10556065delinsTGAAA	GRCh38
NC_000006.11:g.10556294_10556298delinsTGAAA , CM000668.1:g.10556294_10556298delinsTGAAA	GRCh37
NC_000006.10:g.10664280_10664284delinsTGAAA	NCBI36
NG_007469.3:g.68839_68843delinsTGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-363_-359delinsTGAAA MANE Plus Clinical	ENSP00000314844.3:n.-363_-359delinsTGAAA
ENST00000397423.7:n.484+27220_484+27224delinsTGAAA
ENST00000495262.7:c.925+26225_925+26229delinsTGAAA MANE Select	ENSP00000419411.2:n.925+26225_925+26229delinsTGAAA
ENST00000316170.7:c.-363_-359delinsTGAAA	ENSP00000314844.3:n.-363_-359delinsTGAAA
ENST00000379597.7:c.925+26225_925+26229delinsTGAAA	ENSP00000368917.3:n.925+26225_925+26229delinsTGAAA
ENST00000397423.6:n.484+27220_484+27224delinsTGAAA
ENST00000410107.5:c.67+46903_67+46907delinsTGAAA	ENSP00000386321.1:n.67+46903_67+46907delinsTGAAA
ENST00000461400.1:n.25+26225_25+26229delinsTGAAA
ENST00000474518.1:n.508+27220_508+27224delinsTGAAA
ENST00000475577.5:n.254+28401_254+28405delinsTGAAA
ENST00000485764.1:n.40+26225_40+26229delinsTGAAA
ENST00000489225.5:n.283+63130_283+63134delinsTGAAA
ENST00000489819.5:n.175+34467_175+34471delinsTGAAA
ENST00000495262.5:c.925+26225_925+26229delinsTGAAA	ENSP00000419411.1:n.925+26225_925+26229delinsTGAAA
NM_001491.2:c.-363_-359delinsTGAAA	NP_001482.1:n.-363_-359delinsTGAAA
NM_145649.4:c.925+26225_925+26229delinsTGAAA	NP_663624.1:n.925+26225_925+26229delinsTGAAA
XM_005248997.2:c.-363_-359delinsTGAAA	XP_005249054.1:n.-363_-359delinsTGAAA
XM_005248999.2:c.694+26225_694+26229delinsTGAAA	XP_005249056.1:n.694+26225_694+26229delinsTGAAA
XM_006715052.2:c.925+26225_925+26229delinsTGAAA	XP_006715115.1:n.925+26225_925+26229delinsTGAAA
XM_006715053.2:c.*103_*107delinsTGAAA	XP_006715116.1:n.*103_*107delinsTGAAA
XM_011514465.1:c.926-17069_926-17065delinsTGAAA	XP_011512767.1:n.926-17069_926-17065delinsTGAAA
XM_011514467.1:c.694+26225_694+26229delinsTGAAA	XP_011512769.1:n.694+26225_694+26229delinsTGAAA
XR_926136.1:n.1476+26225_1476+26229delinsTGAAA
XM_005248997.3:c.-363_-359delinsTGAAA	XP_005249054.1:n.-363_-359delinsTGAAA
XM_006715052.3:c.925+26225_925+26229delinsTGAAA	XP_006715115.1:n.925+26225_925+26229delinsTGAAA
XR_002956275.1:n.1476+26225_1476+26229delinsTGAAA
XR_926136.2:n.1474+26225_1474+26229delinsTGAAA
NM_001374747.1:c.925+26225_925+26229delinsTGAAA	NP_001361676.1:n.925+26225_925+26229delinsTGAAA
NM_001491.3:c.-363_-359delinsTGAAA MANE Plus Clinical	NP_001482.1:n.-363_-359delinsTGAAA
NM_145649.5:c.925+26225_925+26229delinsTGAAA MANE Select	NP_663624.1:n.925+26225_925+26229delinsTGAAA