Canonical Allele Identifier: CA1610029527

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529682_10529685delinsCATG , CM000668.2:g.10529682_10529685delinsCATG	GRCh38
NC_000006.11:g.10529915_10529918delinsCATG , CM000668.1:g.10529915_10529918delinsCATG	GRCh37
NC_000006.10:g.10637901_10637904delinsCATG	NCBI36
NG_007469.3:g.42460_42463delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+841_484+844delinsCATG
ENST00000495262.7:c.771_774delinsCATG MANE Select	ENSP00000419411.2:p.Asp257=
ENST00000379597.7:c.771_774delinsCATG	ENSP00000368917.3:p.Asp257=
ENST00000397423.6:n.484+841_484+844delinsCATG
ENST00000410107.5:c.67+20524_67+20527delinsCATG	ENSP00000386321.1:n.67+20524_67+20527delinsCATG
ENST00000474518.1:n.508+841_508+844delinsCATG
ENST00000474983.5:n.1348_1351delinsCATG
ENST00000475577.5:n.254+2022_254+2025delinsCATG
ENST00000483204.1:n.1347_1350delinsCATG
ENST00000489225.5:n.283+36751_283+36754delinsCATG
ENST00000489819.5:n.175+8088_175+8091delinsCATG
ENST00000495262.5:c.771_774delinsCATG	ENSP00000419411.1:p.Asp257=
NM_145649.4:c.771_774delinsCATG	NP_663624.1:p.Asp257=
XM_005248999.2:c.540_543delinsCATG	XP_005249056.1:p.Asp180=
XM_006715052.2:c.771_774delinsCATG	XP_006715115.1:p.Asp257=
XM_006715053.2:c.771_774delinsCATG	XP_006715116.1:p.Asp257=
XM_011514465.1:c.771_774delinsCATG	XP_011512767.1:p.Asp257=
XM_011514467.1:c.540_543delinsCATG	XP_011512769.1:p.Asp180=
XM_011514468.1:c.771_774delinsCATG	XP_011512770.1:p.Asp257=
XR_926136.1:n.1322_1325delinsCATG
XM_006715052.3:c.771_774delinsCATG	XP_006715115.1:p.Asp257=
XM_011514468.3:c.771_774delinsCATG	XP_011512770.1:p.Asp257=
XM_017010732.2:c.771_774delinsCATG	XP_016866221.1:p.Asp257=
XR_002956275.1:n.1322_1325delinsCATG
XR_926136.2:n.1320_1323delinsCATG
NM_001374747.1:c.771_774delinsCATG	NP_001361676.1:p.Asp257=
NM_145649.5:c.771_774delinsCATG MANE Select	NP_663624.1:p.Asp257=