Canonical Allele Identifier: CA2677293779

Gene: GCNT2

Linked Data

• gnomAD v4: 6-10556015-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556015C>G , CM000668.2:g.10556015C>G	GRCh38
NC_000006.11:g.10556248C>G , CM000668.1:g.10556248C>G	GRCh37
NC_000006.10:g.10664234C>G	NCBI36
NG_007469.3:g.68793C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-409C>G MANE Plus Clinical	ENSP00000314844.3:n.-409C>G
ENST00000397423.7:n.484+27174C>G
ENST00000495262.7:c.925+26179C>G MANE Select	ENSP00000419411.2:n.925+26179C>G
ENST00000316170.7:c.-409C>G	ENSP00000314844.3:n.-409C>G
ENST00000379597.7:c.925+26179C>G	ENSP00000368917.3:n.925+26179C>G
ENST00000397423.6:n.484+27174C>G
ENST00000410107.5:c.67+46857C>G	ENSP00000386321.1:n.67+46857C>G
ENST00000461400.1:n.25+26179C>G
ENST00000474518.1:n.508+27174C>G
ENST00000475577.5:n.254+28355C>G
ENST00000485764.1:n.40+26179C>G
ENST00000489225.5:n.283+63084C>G
ENST00000489819.5:n.175+34421C>G
ENST00000495262.5:c.925+26179C>G	ENSP00000419411.1:n.925+26179C>G
NM_001491.2:c.-409C>G	NP_001482.1:n.-409C>G
NM_145649.4:c.925+26179C>G	NP_663624.1:n.925+26179C>G
XM_005248997.2:c.-409C>G	XP_005249054.1:n.-409C>G
XM_005248999.2:c.694+26179C>G	XP_005249056.1:n.694+26179C>G
XM_006715052.2:c.925+26179C>G	XP_006715115.1:n.925+26179C>G
XM_006715053.2:c.*57C>G	XP_006715116.1:n.*57C>G
XM_011514465.1:c.926-17115C>G	XP_011512767.1:n.926-17115C>G
XM_011514467.1:c.694+26179C>G	XP_011512769.1:n.694+26179C>G
XR_926136.1:n.1476+26179C>G
XM_005248997.3:c.-409C>G	XP_005249054.1:n.-409C>G
XM_006715052.3:c.925+26179C>G	XP_006715115.1:n.925+26179C>G
XR_002956275.1:n.1476+26179C>G
XR_926136.2:n.1474+26179C>G
NM_001374747.1:c.925+26179C>G	NP_001361676.1:n.925+26179C>G
NM_001491.3:c.-409C>G MANE Plus Clinical	NP_001482.1:n.-409C>G
NM_145649.5:c.925+26179C>G MANE Select	NP_663624.1:n.925+26179C>G