Canonical Allele Identifier: CA2710973288

Gene: GCNT2

Linked Data

• dbSNP Id: rs2113661440

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556662_10556665dup , CM000668.2:g.10556662_10556665dup	GRCh38
NC_000006.11:g.10556895_10556898dup , CM000668.1:g.10556895_10556898dup	GRCh37
NC_000006.10:g.10664881_10664884dup	NCBI36
NG_007469.3:g.69440_69443dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.239_242dup MANE Plus Clinical	ENSP00000314844.3:p.Tyr81Ter
ENST00000397423.7:n.484+27821_484+27824dup
ENST00000495262.7:c.925+26826_925+26829dup MANE Select	ENSP00000419411.2:n.925+26826_925+26829dup
ENST00000640968.1:c.239_242dup	ENSP00000492466.1:p.Tyr81Ter
ENST00000316170.7:c.239_242dup	ENSP00000314844.3:p.Tyr81Ter
ENST00000379597.7:c.925+26826_925+26829dup	ENSP00000368917.3:n.925+26826_925+26829dup
ENST00000397423.6:n.484+27821_484+27824dup
ENST00000410107.5:c.67+47504_67+47507dup	ENSP00000386321.1:n.67+47504_67+47507dup
ENST00000461400.1:n.25+26826_25+26829dup
ENST00000474518.1:n.508+27821_508+27824dup
ENST00000475577.5:n.254+29002_254+29005dup
ENST00000485764.1:n.40+26826_40+26829dup
ENST00000489225.5:n.283+63731_283+63734dup
ENST00000489819.5:n.175+35068_175+35071dup
ENST00000495262.5:c.925+26826_925+26829dup	ENSP00000419411.1:n.925+26826_925+26829dup
NM_001491.2:c.239_242dup	NP_001482.1:p.Tyr81Ter
NM_145649.4:c.925+26826_925+26829dup	NP_663624.1:n.925+26826_925+26829dup
XM_005248997.2:c.239_242dup	XP_005249054.1:p.Tyr81Ter
XM_005248999.2:c.694+26826_694+26829dup	XP_005249056.1:n.694+26826_694+26829dup
XM_006715052.2:c.925+26826_925+26829dup	XP_006715115.1:n.925+26826_925+26829dup
XM_011514465.1:c.926-16468_926-16465dup	XP_011512767.1:n.926-16468_926-16465dup
XM_011514467.1:c.694+26826_694+26829dup	XP_011512769.1:n.694+26826_694+26829dup
XR_926136.1:n.1476+26826_1476+26829dup
XM_005248997.3:c.239_242dup	XP_005249054.1:p.Tyr81Ter
XM_006715052.3:c.925+26826_925+26829dup	XP_006715115.1:n.925+26826_925+26829dup
XR_002956275.1:n.1476+26826_1476+26829dup
XR_926136.2:n.1474+26826_1474+26829dup
NM_001374747.1:c.925+26826_925+26829dup	NP_001361676.1:n.925+26826_925+26829dup
NM_001491.3:c.239_242dup MANE Plus Clinical	NP_001482.1:p.Tyr81Ter
NM_145649.5:c.925+26826_925+26829dup MANE Select	NP_663624.1:n.925+26826_925+26829dup