Canonical Allele Identifier: CA1821104783

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133270_133133284delinsCCTAGCTTTGCAGTG , CM000670.2:g.133133270_133133284delinsCCTAGCTTTGCAGTG	GRCh38
NC_000008.10:g.134145514_134145528delinsCCTAGCTTTGCAGTG , CM000670.1:g.134145514_134145528delinsCCTAGCTTTGCAGTG	GRCh37
NC_000008.9:g.134214696_134214710delinsCCTAGCTTTGCAGTG	NCBI36
NG_015832.1:g.271310_271324delinsCCTAGCTTTGCAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-200_7998-186delinsCCTAGCTTTGCAGTG MANE Select	ENSP00000220616.4:n.7998-200_7998-186deli...
ENST00000220616.8:c.7998-200_7998-186delinsCCTAGCTTTGCAGTG	ENSP00000220616.4:n.7998-200_7998-186deli...
ENST00000519178.5:c.3364-200_3364-186delinsCCTAGCTTTGCAGTG
ENST00000519543.5:c.2397-200_2397-186delinsCCTAGCTTTGCAGTG	ENSP00000430430.1:n.2397-200_2397-186deli...
ENST00000521107.1:c.210-200_210-186delinsCCTAGCTTTGCAGTG	ENSP00000430161.1:n.210-200_210-186delins...
ENST00000523756.5:c.4653-200_4653-186delinsCCTAGCTTTGCAGTG
NM_003235.4:c.7998-200_7998-186delinsCCTAGCTTTGCAGTG	NP_003226.4:n.7998-200_7998-186delinsCCTA...
XM_005251038.3:c.7806-200_7806-186delinsCCTAGCTTTGCAGTG	XP_005251095.1:n.7806-200_7806-186delinsC...
XM_006716622.2:c.7935-200_7935-186delinsCCTAGCTTTGCAGTG	XP_006716685.1:n.7935-200_7935-186delinsC...
XM_005251038.4:c.7806-200_7806-186delinsCCTAGCTTTGCAGTG	XP_005251095.1:n.7806-200_7806-186delinsC...
XM_006716622.3:c.7935-200_7935-186delinsCCTAGCTTTGCAGTG	XP_006716685.1:n.7935-200_7935-186delinsC...
XM_017013793.1:c.7932-200_7932-186delinsCCTAGCTTTGCAGTG	XP_016869282.1:n.7932-200_7932-186delinsC...
XM_017013794.1:c.7863-200_7863-186delinsCCTAGCTTTGCAGTG	XP_016869283.1:n.7863-200_7863-186delinsC...
XM_017013795.1:c.7827-200_7827-186delinsCCTAGCTTTGCAGTG	XP_016869284.1:n.7827-200_7827-186delinsC...
XM_017013796.1:c.7779-200_7779-186delinsCCTAGCTTTGCAGTG	XP_016869285.1:n.7779-200_7779-186delinsC...
XM_017013797.1:c.7737-200_7737-186delinsCCTAGCTTTGCAGTG	XP_016869286.1:n.7737-200_7737-186delinsC...
NM_003235.5:c.7998-200_7998-186delinsCCTAGCTTTGCAGTG MANE Select	NP_003226.4:n.7998-200_7998-186delinsCCTA...