Canonical Allele Identifier: CA2535317080

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529208_10529210del , CM000668.2:g.10529208_10529210del	GRCh38
NC_000006.11:g.10529441_10529443del , CM000668.1:g.10529441_10529443del	GRCh37
NC_000006.10:g.10637427_10637429del	NCBI36
NG_007469.3:g.41986_41988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+367_484+369del
ENST00000483204.2:n.873_875del
ENST00000495262.7:c.297_299del MANE Select	ENSP00000419411.2:p.Tyr99Ter
ENST00000379597.7:c.297_299del	ENSP00000368917.3:p.Tyr99Ter
ENST00000397423.6:n.484+367_484+369del
ENST00000410107.5:c.67+20050_67+20052del	ENSP00000386321.1:n.67+20050_67+20052del
ENST00000474518.1:n.508+367_508+369del
ENST00000474983.5:n.874_876del
ENST00000475577.5:n.254+1548_254+1550del
ENST00000483204.1:n.873_875del
ENST00000489225.5:n.283+36277_283+36279del
ENST00000489819.5:n.175+7614_175+7616del
ENST00000495262.5:c.297_299del	ENSP00000419411.1:p.Tyr99Ter
NM_145649.4:c.297_299del	NP_663624.1:p.Tyr99Ter
XM_005248999.2:c.66_68del	XP_005249056.1:p.Tyr22Ter
XM_006715052.2:c.297_299del	XP_006715115.1:p.Tyr99Ter
XM_006715053.2:c.297_299del	XP_006715116.1:p.Tyr99Ter
XM_011514465.1:c.297_299del	XP_011512767.1:p.Tyr99Ter
XM_011514467.1:c.66_68del	XP_011512769.1:p.Tyr22Ter
XM_011514468.1:c.297_299del	XP_011512770.1:p.Tyr99Ter
XR_926136.1:n.848_850del
XM_006715052.3:c.297_299del	XP_006715115.1:p.Tyr99Ter
XM_011514468.3:c.297_299del	XP_011512770.1:p.Tyr99Ter
XM_017010732.2:c.297_299del	XP_016866221.1:p.Tyr99Ter
XR_002956275.1:n.848_850del
XR_926136.2:n.846_848del
NM_001374747.1:c.297_299del	NP_001361676.1:p.Tyr99Ter
NM_145649.5:c.297_299del MANE Select	NP_663624.1:p.Tyr99Ter