Canonical Allele Identifier: CA645556768

Gene: GCNT2

Linked Data

• COSMIC: COSM6439996

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529836_10529837delinsAA , CM000668.2:g.10529836_10529837delinsAA	GRCh38
NC_000006.11:g.10530069_10530070delinsAA , CM000668.1:g.10530069_10530070delinsAA	GRCh37
NC_000006.10:g.10638055_10638056delinsAA	NCBI36
NG_007469.3:g.42614_42615delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+995_484+996delinsAA
ENST00000495262.7:c.925_925+1delinsAA
ENST00000379597.7:c.925_925+1delinsAA
ENST00000397423.6:n.484+995_484+996delinsAA
ENST00000410107.5:c.67+20678_67+20679delinsAA	ENSP00000386321.1:n.67+20678_67+20679delinsAA
ENST00000461400.1:n.25_25+1delinsAA
ENST00000474518.1:n.508+995_508+996delinsAA
ENST00000474983.5:n.1502_1503delinsAA
ENST00000475577.5:n.254+2176_254+2177delinsAA
ENST00000483204.1:n.1501_1502delinsAA
ENST00000485764.1:n.40_40+1delinsAA
ENST00000489225.5:n.283+36905_283+36906delinsAA
ENST00000489819.5:n.175+8242_175+8243delinsAA
ENST00000495262.5:c.925_925+1delinsAA
NM_145649.4:c.925_925+1delinsAA
XM_005248999.2:c.694_694+1delinsAA
XM_006715052.2:c.925_925+1delinsAA
XM_006715053.2:c.925_925+1delinsAA
XM_011514465.1:c.925_925+1delinsAA
XM_011514467.1:c.694_694+1delinsAA
XM_011514468.1:c.925_925+1delinsAA
XR_926136.1:n.1476_1476+1delinsAA
XM_006715052.3:c.925_925+1delinsAA
XM_011514468.3:c.925_925+1delinsAA
XM_017010732.2:c.925_925+1delinsAA
XR_002956275.1:n.1476_1476+1delinsAA
XR_926136.2:n.1474_1474+1delinsAA
NM_001374747.1:c.925_925+1delinsAA
NM_145649.5:c.925_925+1delinsAA