Canonical Allele Identifier: CA2677293808

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10556043-C-CGGGGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556046_10556051dup , CM000668.2:g.10556046_10556051dup	GRCh38
NC_000006.11:g.10556279_10556284dup , CM000668.1:g.10556279_10556284dup	GRCh37
NC_000006.10:g.10664265_10664270dup	NCBI36
NG_007469.3:g.68824_68829dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-378_-373dup MANE Plus Clinical	ENSP00000314844.3:n.-378_-373dup
ENST00000397423.7:n.484+27205_484+27210dup
ENST00000495262.7:c.925+26210_925+26215dup MANE Select	ENSP00000419411.2:n.925+26210_925+26215dup
ENST00000316170.7:c.-378_-373dup	ENSP00000314844.3:n.-378_-373dup
ENST00000379597.7:c.925+26210_925+26215dup	ENSP00000368917.3:n.925+26210_925+26215dup
ENST00000397423.6:n.484+27205_484+27210dup
ENST00000410107.5:c.67+46888_67+46893dup	ENSP00000386321.1:n.67+46888_67+46893dup
ENST00000461400.1:n.25+26210_25+26215dup
ENST00000474518.1:n.508+27205_508+27210dup
ENST00000475577.5:n.254+28386_254+28391dup
ENST00000485764.1:n.40+26210_40+26215dup
ENST00000489225.5:n.283+63115_283+63120dup
ENST00000489819.5:n.175+34452_175+34457dup
ENST00000495262.5:c.925+26210_925+26215dup	ENSP00000419411.1:n.925+26210_925+26215dup
NM_001491.2:c.-378_-373dup	NP_001482.1:n.-378_-373dup
NM_145649.4:c.925+26210_925+26215dup	NP_663624.1:n.925+26210_925+26215dup
XM_005248997.2:c.-378_-373dup	XP_005249054.1:n.-378_-373dup
XM_005248999.2:c.694+26210_694+26215dup	XP_005249056.1:n.694+26210_694+26215dup
XM_006715052.2:c.925+26210_925+26215dup	XP_006715115.1:n.925+26210_925+26215dup
XM_006715053.2:c.*88_*93dup	XP_006715116.1:n.*88_*93dup
XM_011514465.1:c.926-17084_926-17079dup	XP_011512767.1:n.926-17084_926-17079dup
XM_011514467.1:c.694+26210_694+26215dup	XP_011512769.1:n.694+26210_694+26215dup
XR_926136.1:n.1476+26210_1476+26215dup
XM_005248997.3:c.-378_-373dup	XP_005249054.1:n.-378_-373dup
XM_006715052.3:c.925+26210_925+26215dup	XP_006715115.1:n.925+26210_925+26215dup
XR_002956275.1:n.1476+26210_1476+26215dup
XR_926136.2:n.1474+26210_1474+26215dup
NM_001374747.1:c.925+26210_925+26215dup	NP_001361676.1:n.925+26210_925+26215dup
NM_001491.3:c.-378_-373dup MANE Plus Clinical	NP_001482.1:n.-378_-373dup
NM_145649.5:c.925+26210_925+26215dup MANE Select	NP_663624.1:n.925+26210_925+26215dup