Canonical Allele Identifier: CA1085909444

Gene: GCNT2

Linked Data

• dbSNP Id: rs1761393648
• gnomAD v3: 6-10529800-GACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT-G
• gnomAD v4: 6-10529800-GACGAACATTTCTGGGTGACACTCAACAGGATTCCCGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529802_10529839del , CM000668.2:g.10529802_10529839del	GRCh38
NC_000006.11:g.10530035_10530072del , CM000668.1:g.10530035_10530072del	GRCh37
NC_000006.10:g.10638021_10638058del	NCBI36
NG_007469.3:g.42580_42617del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+961_484+998del
ENST00000495262.7:c.891_925+3del
ENST00000379597.7:c.891_925+3del
ENST00000397423.6:n.484+961_484+998del
ENST00000410107.5:c.67+20644_67+20681del	ENSP00000386321.1:n.67+20644_67+20681del
ENST00000474518.1:n.508+961_508+998del
ENST00000474983.5:n.1468_1505del
ENST00000475577.5:n.254+2142_254+2179del
ENST00000483204.1:n.1467_1504del
ENST00000485764.1:n.6_40+3del
ENST00000489225.5:n.283+36871_283+36908del
ENST00000489819.5:n.175+8208_175+8245del
ENST00000495262.5:c.891_925+3del
NM_145649.4:c.891_925+3del
XM_005248999.2:c.660_694+3del
XM_006715052.2:c.891_925+3del
XM_006715053.2:c.891_925+3del
XM_011514465.1:c.891_925+3del
XM_011514467.1:c.660_694+3del
XM_011514468.1:c.891_925+3del
XR_926136.1:n.1442_1476+3del
XM_006715052.3:c.891_925+3del
XM_011514468.3:c.891_925+3del
XM_017010732.2:c.891_925+3del
XR_002956275.1:n.1442_1476+3del
XR_926136.2:n.1440_1474+3del
NM_001374747.1:c.891_925+3del
NM_145649.5:c.891_925+3del