Canonical Allele Identifier: CA2677293142

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10529861-TTTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529862_10529865del , CM000668.2:g.10529862_10529865del	GRCh38
NC_000006.11:g.10530095_10530098del , CM000668.1:g.10530095_10530098del	GRCh37
NC_000006.10:g.10638081_10638084del	NCBI36
NG_007469.3:g.42640_42643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+1021_484+1024del
ENST00000495262.7:c.925+26_925+29del MANE Select	ENSP00000419411.2:n.925+26_925+29del
ENST00000379597.7:c.925+26_925+29del	ENSP00000368917.3:n.925+26_925+29del
ENST00000397423.6:n.484+1021_484+1024del
ENST00000410107.5:c.67+20704_67+20707del	ENSP00000386321.1:n.67+20704_67+20707del
ENST00000461400.1:n.25+26_25+29del
ENST00000474518.1:n.508+1021_508+1024del
ENST00000474983.5:n.1528_1531del
ENST00000475577.5:n.254+2202_254+2205del
ENST00000483204.1:n.1527_1530del
ENST00000485764.1:n.40+26_40+29del
ENST00000489225.5:n.283+36931_283+36934del
ENST00000489819.5:n.175+8268_175+8271del
ENST00000495262.5:c.925+26_925+29del	ENSP00000419411.1:n.925+26_925+29del
NM_145649.4:c.925+26_925+29del	NP_663624.1:n.925+26_925+29del
XM_005248999.2:c.694+26_694+29del	XP_005249056.1:n.694+26_694+29del
XM_006715052.2:c.925+26_925+29del	XP_006715115.1:n.925+26_925+29del
XM_006715053.2:c.925+26_925+29del	XP_006715116.1:n.925+26_925+29del
XM_011514465.1:c.925+26_925+29del	XP_011512767.1:n.925+26_925+29del
XM_011514467.1:c.694+26_694+29del	XP_011512769.1:n.694+26_694+29del
XM_011514468.1:c.925+26_925+29del	XP_011512770.1:n.925+26_925+29del
XR_926136.1:n.1476+26_1476+29del
XM_006715052.3:c.925+26_925+29del	XP_006715115.1:n.925+26_925+29del
XM_011514468.3:c.925+26_925+29del	XP_011512770.1:n.925+26_925+29del
XM_017010732.2:c.925+26_925+29del	XP_016866221.1:n.925+26_925+29del
XR_002956275.1:n.1476+26_1476+29del
XR_926136.2:n.1474+26_1474+29del
NM_001374747.1:c.925+26_925+29del	NP_001361676.1:n.925+26_925+29del
NM_145649.5:c.925+26_925+29del MANE Select	NP_663624.1:n.925+26_925+29del