Canonical Allele Identifier: CA2677294107

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10556605-A-AAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556610_10556613dup , CM000668.2:g.10556610_10556613dup	GRCh38
NC_000006.11:g.10556843_10556846dup , CM000668.1:g.10556843_10556846dup	GRCh37
NC_000006.10:g.10664829_10664832dup	NCBI36
NG_007469.3:g.69388_69391dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.187_190dup MANE Plus Clinical	ENSP00000314844.3:p.Leu64GlnfsTer6
ENST00000397423.7:n.484+27769_484+27772dup
ENST00000495262.7:c.925+26774_925+26777dup MANE Select	ENSP00000419411.2:n.925+26774_925+26777dup
ENST00000640968.1:c.187_190dup	ENSP00000492466.1:p.Leu64GlnfsTer6
ENST00000316170.7:c.187_190dup	ENSP00000314844.3:p.Leu64GlnfsTer6
ENST00000379597.7:c.925+26774_925+26777dup	ENSP00000368917.3:n.925+26774_925+26777dup
ENST00000397423.6:n.484+27769_484+27772dup
ENST00000410107.5:c.67+47452_67+47455dup	ENSP00000386321.1:n.67+47452_67+47455dup
ENST00000461400.1:n.25+26774_25+26777dup
ENST00000474518.1:n.508+27769_508+27772dup
ENST00000475577.5:n.254+28950_254+28953dup
ENST00000485764.1:n.40+26774_40+26777dup
ENST00000489225.5:n.283+63679_283+63682dup
ENST00000489819.5:n.175+35016_175+35019dup
ENST00000495262.5:c.925+26774_925+26777dup	ENSP00000419411.1:n.925+26774_925+26777dup
NM_001491.2:c.187_190dup	NP_001482.1:p.Leu64GlnfsTer6
NM_145649.4:c.925+26774_925+26777dup	NP_663624.1:n.925+26774_925+26777dup
XM_005248997.2:c.187_190dup	XP_005249054.1:p.Leu64GlnfsTer6
XM_005248999.2:c.694+26774_694+26777dup	XP_005249056.1:n.694+26774_694+26777dup
XM_006715052.2:c.925+26774_925+26777dup	XP_006715115.1:n.925+26774_925+26777dup
XM_011514465.1:c.926-16520_926-16517dup	XP_011512767.1:n.926-16520_926-16517dup
XM_011514467.1:c.694+26774_694+26777dup	XP_011512769.1:n.694+26774_694+26777dup
XR_926136.1:n.1476+26774_1476+26777dup
XM_005248997.3:c.187_190dup	XP_005249054.1:p.Leu64GlnfsTer6
XM_006715052.3:c.925+26774_925+26777dup	XP_006715115.1:n.925+26774_925+26777dup
XR_002956275.1:n.1476+26774_1476+26777dup
XR_926136.2:n.1474+26774_1474+26777dup
NM_001374747.1:c.925+26774_925+26777dup	NP_001361676.1:n.925+26774_925+26777dup
NM_001491.3:c.187_190dup MANE Plus Clinical	NP_001482.1:p.Leu64GlnfsTer6
NM_145649.5:c.925+26774_925+26777dup MANE Select	NP_663624.1:n.925+26774_925+26777dup