Canonical Allele Identifier: CA362709134

Gene: GCNT2

Linked Data

• MyVariant Identifiers: chr6:g.10529918G>A (hg19) ; chr6:g.10529685G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529685G>A , CM000668.2:g.10529685G>A	GRCh38
NC_000006.11:g.10529918G>A , CM000668.1:g.10529918G>A	GRCh37
NC_000006.10:g.10637904G>A	NCBI36
NG_007469.3:g.42463G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+844G>A
ENST00000495262.7:c.774G>A MANE Select	ENSP00000419411.2:p.Met258Ile
ENST00000379597.7:c.774G>A	ENSP00000368917.3:p.Met258Ile
ENST00000397423.6:n.484+844G>A
ENST00000410107.5:c.67+20527G>A	ENSP00000386321.1:n.67+20527G>A
ENST00000474518.1:n.508+844G>A
ENST00000474983.5:n.1351G>A
ENST00000475577.5:n.254+2025G>A
ENST00000483204.1:n.1350G>A
ENST00000489225.5:n.283+36754G>A
ENST00000489819.5:n.175+8091G>A
ENST00000495262.5:c.774G>A	ENSP00000419411.1:p.Met258Ile
NM_145649.4:c.774G>A	NP_663624.1:p.Met258Ile
XM_005248999.2:c.543G>A	XP_005249056.1:p.Met181Ile
XM_006715052.2:c.774G>A	XP_006715115.1:p.Met258Ile
XM_006715053.2:c.774G>A	XP_006715116.1:p.Met258Ile
XM_011514465.1:c.774G>A	XP_011512767.1:p.Met258Ile
XM_011514467.1:c.543G>A	XP_011512769.1:p.Met181Ile
XM_011514468.1:c.774G>A	XP_011512770.1:p.Met258Ile
XR_926136.1:n.1325G>A
XM_006715052.3:c.774G>A	XP_006715115.1:p.Met258Ile
XM_011514468.3:c.774G>A	XP_011512770.1:p.Met258Ile
XM_017010732.2:c.774G>A	XP_016866221.1:p.Met258Ile
XR_002956275.1:n.1325G>A
XR_926136.2:n.1323G>A
NM_001374747.1:c.774G>A	NP_001361676.1:p.Met258Ile
NM_145649.5:c.774G>A MANE Select	NP_663624.1:p.Met258Ile