Canonical Allele Identifier: CA1821104821

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133349_133133350delinsCT , CM000670.2:g.133133349_133133350delinsCT	GRCh38
NC_000008.10:g.134145593_134145594delinsCT , CM000670.1:g.134145593_134145594delinsCT	GRCh37
NC_000008.9:g.134214775_134214776delinsCT	NCBI36
NG_015832.1:g.271389_271390delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-121_7998-120delinsCT MANE Select	ENSP00000220616.4:n.7998-121_7998-120delinsCT
ENST00000220616.8:c.7998-121_7998-120delinsCT	ENSP00000220616.4:n.7998-121_7998-120delinsCT
ENST00000519178.5:c.3364-121_3364-120delinsCT
ENST00000519543.5:c.2397-121_2397-120delinsCT	ENSP00000430430.1:n.2397-121_2397-120delinsCT
ENST00000521107.1:c.210-121_210-120delinsCT	ENSP00000430161.1:n.210-121_210-120delinsCT
ENST00000523756.5:c.4653-121_4653-120delinsCT
NM_003235.4:c.7998-121_7998-120delinsCT	NP_003226.4:n.7998-121_7998-120delinsCT
XM_005251038.3:c.7806-121_7806-120delinsCT	XP_005251095.1:n.7806-121_7806-120delinsCT
XM_006716622.2:c.7935-121_7935-120delinsCT	XP_006716685.1:n.7935-121_7935-120delinsCT
XM_005251038.4:c.7806-121_7806-120delinsCT	XP_005251095.1:n.7806-121_7806-120delinsCT
XM_006716622.3:c.7935-121_7935-120delinsCT	XP_006716685.1:n.7935-121_7935-120delinsCT
XM_017013793.1:c.7932-121_7932-120delinsCT	XP_016869282.1:n.7932-121_7932-120delinsCT
XM_017013794.1:c.7863-121_7863-120delinsCT	XP_016869283.1:n.7863-121_7863-120delinsCT
XM_017013795.1:c.7827-121_7827-120delinsCT	XP_016869284.1:n.7827-121_7827-120delinsCT
XM_017013796.1:c.7779-121_7779-120delinsCT	XP_016869285.1:n.7779-121_7779-120delinsCT
XM_017013797.1:c.7737-121_7737-120delinsCT	XP_016869286.1:n.7737-121_7737-120delinsCT
NM_003235.5:c.7998-121_7998-120delinsCT MANE Select	NP_003226.4:n.7998-121_7998-120delinsCT