Canonical Allele Identifier: CA816672868

Gene: GCNT2

Linked Data

• dbSNP Id: rs1465530782
• gnomAD v3: 6-10556061-TGAAA-T
• gnomAD v4: 6-10556061-TGAAA-T
• MyVariant Identifiers: chr6:g.10556295_10556298del (hg19) ; chr6:g.10556062_10556065del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556068_10556071del , CM000668.2:g.10556068_10556071del	GRCh38
NC_000006.11:g.10556301_10556304del , CM000668.1:g.10556301_10556304del	GRCh37
NC_000006.10:g.10664287_10664290del	NCBI36
NG_007469.3:g.68846_68849del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-356_-353del MANE Plus Clinical	ENSP00000314844.3:n.-356_-353del
ENST00000397423.7:n.484+27227_484+27230del
ENST00000495262.7:c.925+26232_925+26235del MANE Select	ENSP00000419411.2:n.925+26232_925+26235del
ENST00000316170.7:c.-356_-353del	ENSP00000314844.3:n.-356_-353del
ENST00000379597.7:c.925+26232_925+26235del	ENSP00000368917.3:n.925+26232_925+26235del
ENST00000397423.6:n.484+27227_484+27230del
ENST00000410107.5:c.67+46910_67+46913del	ENSP00000386321.1:n.67+46910_67+46913del
ENST00000461400.1:n.25+26232_25+26235del
ENST00000474518.1:n.508+27227_508+27230del
ENST00000475577.5:n.254+28408_254+28411del
ENST00000485764.1:n.40+26232_40+26235del
ENST00000489225.5:n.283+63137_283+63140del
ENST00000489819.5:n.175+34474_175+34477del
ENST00000495262.5:c.925+26232_925+26235del	ENSP00000419411.1:n.925+26232_925+26235del
NM_001491.2:c.-356_-353del	NP_001482.1:n.-356_-353del
NM_145649.4:c.925+26232_925+26235del	NP_663624.1:n.925+26232_925+26235del
XM_005248997.2:c.-356_-353del	XP_005249054.1:n.-356_-353del
XM_005248999.2:c.694+26232_694+26235del	XP_005249056.1:n.694+26232_694+26235del
XM_006715052.2:c.925+26232_925+26235del	XP_006715115.1:n.925+26232_925+26235del
XM_006715053.2:c.*110_*113del	XP_006715116.1:n.*110_*113del
XM_011514465.1:c.926-17062_926-17059del	XP_011512767.1:n.926-17062_926-17059del
XM_011514467.1:c.694+26232_694+26235del	XP_011512769.1:n.694+26232_694+26235del
XR_926136.1:n.1476+26232_1476+26235del
XM_005248997.3:c.-356_-353del	XP_005249054.1:n.-356_-353del
XM_006715052.3:c.925+26232_925+26235del	XP_006715115.1:n.925+26232_925+26235del
XR_002956275.1:n.1476+26232_1476+26235del
XR_926136.2:n.1474+26232_1474+26235del
NM_001374747.1:c.925+26232_925+26235del	NP_001361676.1:n.925+26232_925+26235del
NM_001491.3:c.-356_-353del MANE Plus Clinical	NP_001482.1:n.-356_-353del
NM_145649.5:c.925+26232_925+26235del MANE Select	NP_663624.1:n.925+26232_925+26235del