Canonical Allele Identifier: CA816672872

Gene: GCNT2

Linked Data

• dbSNP Id: rs1267675960
• gnomAD v4: 6-10556068-AAG-A
• MyVariant Identifiers: chr6:g.10556302_10556303del (hg19) ; chr6:g.10556069_10556070del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556072_10556073del , CM000668.2:g.10556072_10556073del	GRCh38
NC_000006.11:g.10556305_10556306del , CM000668.1:g.10556305_10556306del	GRCh37
NC_000006.10:g.10664291_10664292del	NCBI36
NG_007469.3:g.68850_68851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-352_-351del MANE Plus Clinical	ENSP00000314844.3:n.-352_-351del
ENST00000397423.7:n.484+27231_484+27232del
ENST00000495262.7:c.925+26236_925+26237del MANE Select	ENSP00000419411.2:n.925+26236_925+26237del
ENST00000316170.7:c.-352_-351del	ENSP00000314844.3:n.-352_-351del
ENST00000379597.7:c.925+26236_925+26237del	ENSP00000368917.3:n.925+26236_925+26237del
ENST00000397423.6:n.484+27231_484+27232del
ENST00000410107.5:c.67+46914_67+46915del	ENSP00000386321.1:n.67+46914_67+46915del
ENST00000461400.1:n.25+26236_25+26237del
ENST00000474518.1:n.508+27231_508+27232del
ENST00000475577.5:n.254+28412_254+28413del
ENST00000485764.1:n.40+26236_40+26237del
ENST00000489225.5:n.283+63141_283+63142del
ENST00000489819.5:n.175+34478_175+34479del
ENST00000495262.5:c.925+26236_925+26237del	ENSP00000419411.1:n.925+26236_925+26237del
NM_001491.2:c.-352_-351del	NP_001482.1:n.-352_-351del
NM_145649.4:c.925+26236_925+26237del	NP_663624.1:n.925+26236_925+26237del
XM_005248997.2:c.-352_-351del	XP_005249054.1:n.-352_-351del
XM_005248999.2:c.694+26236_694+26237del	XP_005249056.1:n.694+26236_694+26237del
XM_006715052.2:c.925+26236_925+26237del	XP_006715115.1:n.925+26236_925+26237del
XM_006715053.2:c.*114_*115del	XP_006715116.1:n.*114_*115del
XM_011514465.1:c.926-17058_926-17057del	XP_011512767.1:n.926-17058_926-17057del
XM_011514467.1:c.694+26236_694+26237del	XP_011512769.1:n.694+26236_694+26237del
XR_926136.1:n.1476+26236_1476+26237del
XM_005248997.3:c.-352_-351del	XP_005249054.1:n.-352_-351del
XM_006715052.3:c.925+26236_925+26237del	XP_006715115.1:n.925+26236_925+26237del
XR_002956275.1:n.1476+26236_1476+26237del
XR_926136.2:n.1474+26236_1474+26237del
NM_001374747.1:c.925+26236_925+26237del	NP_001361676.1:n.925+26236_925+26237del
NM_001491.3:c.-352_-351del MANE Plus Clinical	NP_001482.1:n.-352_-351del
NM_145649.5:c.925+26236_925+26237del MANE Select	NP_663624.1:n.925+26236_925+26237del