Canonical Allele Identifier: CA2782278446
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133589_133133590insACACAC , CM000670.2:g.133133589_133133590insACACAC GRCh38
NC_000008.10:g.134145833_134145834insACACAC , CM000670.1:g.134145833_134145834insACACAC GRCh37
NC_000008.9:g.134215015_134215016insACACAC NCBI36
NG_015832.1:g.271629_271630insACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8117_8118insACACAC MANE Select ENSP00000220616.4:p.Asn2706delinsLysHisThr
ENST00000220616.8:c.8117_8118insACACAC ENSP00000220616.4:p.Asn2706delinsLysHisThr
ENST00000519178.5:c.3483_3484insACACAC
ENST00000519543.5:c.2516_2517insACACAC ENSP00000430430.1:p.Asn839delinsLysHisThr
ENST00000521107.1:c.329_330insACACAC ENSP00000430161.1:p.Asn110delinsLysHisThr
ENST00000522691.1:n.203_204insACACAC
ENST00000523756.5:c.4772_4773insACACAC
NM_003235.4:c.8117_8118insACACAC NP_003226.4:p.Asn2706delinsLysHisThr
XM_005251038.3:c.7925_7926insACACAC XP_005251095.1:p.Asn2642delinsLysHisThr
XM_006716622.2:c.8054_8055insACACAC XP_006716685.1:p.Asn2685delinsLysHisThr
XM_005251038.4:c.7925_7926insACACAC XP_005251095.1:p.Asn2642delinsLysHisThr
XM_006716622.3:c.8054_8055insACACAC XP_006716685.1:p.Asn2685delinsLysHisThr
XM_017013793.1:c.8051_8052insACACAC XP_016869282.1:p.Asn2684delinsLysHisThr
XM_017013794.1:c.7982_7983insACACAC XP_016869283.1:p.Asn2661delinsLysHisThr
XM_017013795.1:c.7946_7947insACACAC XP_016869284.1:p.Asn2649delinsLysHisThr
XM_017013796.1:c.7898_7899insACACAC XP_016869285.1:p.Asn2633delinsLysHisThr
XM_017013797.1:c.7856_7857insACACAC XP_016869286.1:p.Asn2619delinsLysHisThr
NM_003235.5:c.8117_8118insACACAC MANE Select NP_003226.4:p.Asn2706delinsLysHisThr