Canonical Allele Identifier: CA816672861

Gene: GCNT2

Linked Data

• dbSNP Id: rs1441964939
• gnomAD v4: 6-10556037-A-AG
• MyVariant Identifiers: chr6:g.10556270_10556271insG (hg19) ; chr6:g.10556037_10556038insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556042dup , CM000668.2:g.10556042dup	GRCh38
NC_000006.11:g.10556275dup , CM000668.1:g.10556275dup	GRCh37
NC_000006.10:g.10664261dup	NCBI36
NG_007469.3:g.68820dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-382dup MANE Plus Clinical	ENSP00000314844.3:n.-382dup
ENST00000397423.7:n.484+27201dup
ENST00000495262.7:c.925+26206dup MANE Select	ENSP00000419411.2:n.925+26206dup
ENST00000316170.7:c.-382dup	ENSP00000314844.3:n.-382dup
ENST00000379597.7:c.925+26206dup	ENSP00000368917.3:n.925+26206dup
ENST00000397423.6:n.484+27201dup
ENST00000410107.5:c.67+46884dup	ENSP00000386321.1:n.67+46884dup
ENST00000461400.1:n.25+26206dup
ENST00000474518.1:n.508+27201dup
ENST00000475577.5:n.254+28382dup
ENST00000485764.1:n.40+26206dup
ENST00000489225.5:n.283+63111dup
ENST00000489819.5:n.175+34448dup
ENST00000495262.5:c.925+26206dup	ENSP00000419411.1:n.925+26206dup
NM_001491.2:c.-382dup	NP_001482.1:n.-382dup
NM_145649.4:c.925+26206dup	NP_663624.1:n.925+26206dup
XM_005248997.2:c.-382dup	XP_005249054.1:n.-382dup
XM_005248999.2:c.694+26206dup	XP_005249056.1:n.694+26206dup
XM_006715052.2:c.925+26206dup	XP_006715115.1:n.925+26206dup
XM_006715053.2:c.*84dup	XP_006715116.1:n.*84dup
XM_011514465.1:c.926-17088dup	XP_011512767.1:n.926-17088dup
XM_011514467.1:c.694+26206dup	XP_011512769.1:n.694+26206dup
XR_926136.1:n.1476+26206dup
XM_005248997.3:c.-382dup	XP_005249054.1:n.-382dup
XM_006715052.3:c.925+26206dup	XP_006715115.1:n.925+26206dup
XR_002956275.1:n.1476+26206dup
XR_926136.2:n.1474+26206dup
NM_001374747.1:c.925+26206dup	NP_001361676.1:n.925+26206dup
NM_001491.3:c.-382dup MANE Plus Clinical	NP_001482.1:n.-382dup
NM_145649.5:c.925+26206dup MANE Select	NP_663624.1:n.925+26206dup