Canonical Allele Identifier: CA2677293634

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10555705-ACTCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10555707_10555711del , CM000668.2:g.10555707_10555711del	GRCh38
NC_000006.11:g.10555940_10555944del , CM000668.1:g.10555940_10555944del	GRCh37
NC_000006.10:g.10663926_10663930del	NCBI36
NG_007469.3:g.68485_68489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+26866_484+26870del
ENST00000495262.7:c.925+25871_925+25875del MANE Select	ENSP00000419411.2:n.925+25871_925+25875del
ENST00000379597.7:c.925+25871_925+25875del	ENSP00000368917.3:n.925+25871_925+25875del
ENST00000397423.6:n.484+26866_484+26870del
ENST00000410107.5:c.67+46549_67+46553del	ENSP00000386321.1:n.67+46549_67+46553del
ENST00000461400.1:n.25+25871_25+25875del
ENST00000474518.1:n.508+26866_508+26870del
ENST00000475577.5:n.254+28047_254+28051del
ENST00000485764.1:n.40+25871_40+25875del
ENST00000489225.5:n.283+62776_283+62780del
ENST00000489819.5:n.175+34113_175+34117del
ENST00000495262.5:c.925+25871_925+25875del	ENSP00000419411.1:n.925+25871_925+25875del
NM_145649.4:c.925+25871_925+25875del	NP_663624.1:n.925+25871_925+25875del
XM_005248999.2:c.694+25871_694+25875del	XP_005249056.1:n.694+25871_694+25875del
XM_006715052.2:c.925+25871_925+25875del	XP_006715115.1:n.925+25871_925+25875del
XM_006715053.2:c.926-127_926-123del	XP_006715116.1:n.926-127_926-123del
XM_011514465.1:c.926-17423_926-17419del	XP_011512767.1:n.926-17423_926-17419del
XM_011514467.1:c.694+25871_694+25875del	XP_011512769.1:n.694+25871_694+25875del
XR_926136.1:n.1476+25871_1476+25875del
XM_006715052.3:c.925+25871_925+25875del	XP_006715115.1:n.925+25871_925+25875del
XR_002956275.1:n.1476+25871_1476+25875del
XR_926136.2:n.1474+25871_1474+25875del
NM_001374747.1:c.925+25871_925+25875del	NP_001361676.1:n.925+25871_925+25875del
NM_145649.5:c.925+25871_925+25875del MANE Select	NP_663624.1:n.925+25871_925+25875del