Canonical Allele Identifier: CA2677293164

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10529892-AAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529895_10529897del , CM000668.2:g.10529895_10529897del	GRCh38
NC_000006.11:g.10530128_10530130del , CM000668.1:g.10530128_10530130del	GRCh37
NC_000006.10:g.10638114_10638116del	NCBI36
NG_007469.3:g.42673_42675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+1054_484+1056del
ENST00000495262.7:c.925+59_925+61del MANE Select	ENSP00000419411.2:n.925+59_925+61del
ENST00000379597.7:c.925+59_925+61del	ENSP00000368917.3:n.925+59_925+61del
ENST00000397423.6:n.484+1054_484+1056del
ENST00000410107.5:c.67+20737_67+20739del	ENSP00000386321.1:n.67+20737_67+20739del
ENST00000461400.1:n.25+59_25+61del
ENST00000474518.1:n.508+1054_508+1056del
ENST00000474983.5:n.1561_1563del
ENST00000475577.5:n.254+2235_254+2237del
ENST00000483204.1:n.1560_1562del
ENST00000485764.1:n.40+59_40+61del
ENST00000489225.5:n.283+36964_283+36966del
ENST00000489819.5:n.175+8301_175+8303del
ENST00000495262.5:c.925+59_925+61del	ENSP00000419411.1:n.925+59_925+61del
NM_145649.4:c.925+59_925+61del	NP_663624.1:n.925+59_925+61del
XM_005248999.2:c.694+59_694+61del	XP_005249056.1:n.694+59_694+61del
XM_006715052.2:c.925+59_925+61del	XP_006715115.1:n.925+59_925+61del
XM_006715053.2:c.925+59_925+61del	XP_006715116.1:n.925+59_925+61del
XM_011514465.1:c.925+59_925+61del	XP_011512767.1:n.925+59_925+61del
XM_011514467.1:c.694+59_694+61del	XP_011512769.1:n.694+59_694+61del
XM_011514468.1:c.925+59_925+61del	XP_011512770.1:n.925+59_925+61del
XR_926136.1:n.1476+59_1476+61del
XM_006715052.3:c.925+59_925+61del	XP_006715115.1:n.925+59_925+61del
XM_011514468.3:c.925+59_925+61del	XP_011512770.1:n.925+59_925+61del
XM_017010732.2:c.925+59_925+61del	XP_016866221.1:n.925+59_925+61del
XR_002956275.1:n.1476+59_1476+61del
XR_926136.2:n.1474+59_1474+61del
NM_001374747.1:c.925+59_925+61del	NP_001361676.1:n.925+59_925+61del
NM_145649.5:c.925+59_925+61del MANE Select	NP_663624.1:n.925+59_925+61del