Canonical Allele Identifier: CA1610028609

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556673_10556674delinsGC , CM000668.2:g.10556673_10556674delinsGC	GRCh38
NC_000006.11:g.10556906_10556907delinsGC , CM000668.1:g.10556906_10556907delinsGC	GRCh37
NC_000006.10:g.10664892_10664893delinsGC	NCBI36
NG_007469.3:g.69451_69452delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.250_251delinsGC MANE Plus Clinical	ENSP00000314844.3:p.Ala84=
ENST00000397423.7:n.484+27832_484+27833delinsGC
ENST00000495262.7:c.925+26837_925+26838delinsGC MANE Select	ENSP00000419411.2:n.925+26837_925+26838delinsGC
ENST00000640968.1:c.250_251delinsGC	ENSP00000492466.1:p.Ala84=
ENST00000316170.7:c.250_251delinsGC	ENSP00000314844.3:p.Ala84=
ENST00000379597.7:c.925+26837_925+26838delinsGC	ENSP00000368917.3:n.925+26837_925+26838delinsGC
ENST00000397423.6:n.484+27832_484+27833delinsGC
ENST00000410107.5:c.67+47515_67+47516delinsGC	ENSP00000386321.1:n.67+47515_67+47516delinsGC
ENST00000461400.1:n.25+26837_25+26838delinsGC
ENST00000474518.1:n.508+27832_508+27833delinsGC
ENST00000475577.5:n.254+29013_254+29014delinsGC
ENST00000485764.1:n.40+26837_40+26838delinsGC
ENST00000489225.5:n.283+63742_283+63743delinsGC
ENST00000489819.5:n.175+35079_175+35080delinsGC
ENST00000495262.5:c.925+26837_925+26838delinsGC	ENSP00000419411.1:n.925+26837_925+26838delinsGC
NM_001491.2:c.250_251delinsGC	NP_001482.1:p.Ala84=
NM_145649.4:c.925+26837_925+26838delinsGC	NP_663624.1:n.925+26837_925+26838delinsGC
XM_005248997.2:c.250_251delinsGC	XP_005249054.1:p.Ala84=
XM_005248999.2:c.694+26837_694+26838delinsGC	XP_005249056.1:n.694+26837_694+26838delinsGC
XM_006715052.2:c.925+26837_925+26838delinsGC	XP_006715115.1:n.925+26837_925+26838delinsGC
XM_011514465.1:c.926-16457_926-16456delinsGC	XP_011512767.1:n.926-16457_926-16456delinsGC
XM_011514467.1:c.694+26837_694+26838delinsGC	XP_011512769.1:n.694+26837_694+26838delinsGC
XR_926136.1:n.1476+26837_1476+26838delinsGC
XM_005248997.3:c.250_251delinsGC	XP_005249054.1:p.Ala84=
XM_006715052.3:c.925+26837_925+26838delinsGC	XP_006715115.1:n.925+26837_925+26838delinsGC
XR_002956275.1:n.1476+26837_1476+26838delinsGC
XR_926136.2:n.1474+26837_1474+26838delinsGC
NM_001374747.1:c.925+26837_925+26838delinsGC	NP_001361676.1:n.925+26837_925+26838delinsGC
NM_001491.3:c.250_251delinsGC MANE Plus Clinical	NP_001482.1:p.Ala84=
NM_145649.5:c.925+26837_925+26838delinsGC MANE Select	NP_663624.1:n.925+26837_925+26838delinsGC