Canonical Allele Identifier: CA362708712

Gene: GCNT2

Linked Data

• MyVariant Identifiers: chr6:g.10529740C>A (hg19) ; chr6:g.10529507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529507C>A , CM000668.2:g.10529507C>A	GRCh38
NC_000006.11:g.10529740C>A , CM000668.1:g.10529740C>A	GRCh37
NC_000006.10:g.10637726C>A	NCBI36
NG_007469.3:g.42285C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397423.7:n.484+666C>A
ENST00000495262.7:c.596C>A MANE Select	ENSP00000419411.2:p.Thr199Asn
ENST00000379597.7:c.596C>A	ENSP00000368917.3:p.Thr199Asn
ENST00000397423.6:n.484+666C>A
ENST00000410107.5:c.67+20349C>A	ENSP00000386321.1:n.67+20349C>A
ENST00000474518.1:n.508+666C>A
ENST00000474983.5:n.1173C>A
ENST00000475577.5:n.254+1847C>A
ENST00000483204.1:n.1172C>A
ENST00000489225.5:n.283+36576C>A
ENST00000489819.5:n.175+7913C>A
ENST00000495262.5:c.596C>A	ENSP00000419411.1:p.Thr199Asn
NM_145649.4:c.596C>A	NP_663624.1:p.Thr199Asn
XM_005248999.2:c.365C>A	XP_005249056.1:p.Thr122Asn
XM_006715052.2:c.596C>A	XP_006715115.1:p.Thr199Asn
XM_006715053.2:c.596C>A	XP_006715116.1:p.Thr199Asn
XM_011514465.1:c.596C>A	XP_011512767.1:p.Thr199Asn
XM_011514467.1:c.365C>A	XP_011512769.1:p.Thr122Asn
XM_011514468.1:c.596C>A	XP_011512770.1:p.Thr199Asn
XR_926136.1:n.1147C>A
XM_006715052.3:c.596C>A	XP_006715115.1:p.Thr199Asn
XM_011514468.3:c.596C>A	XP_011512770.1:p.Thr199Asn
XM_017010732.2:c.596C>A	XP_016866221.1:p.Thr199Asn
XR_002956275.1:n.1147C>A
XR_926136.2:n.1145C>A
NM_001374747.1:c.596C>A	NP_001361676.1:p.Thr199Asn
NM_145649.5:c.596C>A MANE Select	NP_663624.1:p.Thr199Asn