Canonical Allele Identifier: CA1821104776

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133258_133133259delinsAC , CM000670.2:g.133133258_133133259delinsAC	GRCh38
NC_000008.10:g.134145502_134145503delinsAC , CM000670.1:g.134145502_134145503delinsAC	GRCh37
NC_000008.9:g.134214684_134214685delinsAC	NCBI36
NG_015832.1:g.271298_271299delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-212_7998-211delinsAC MANE Select	ENSP00000220616.4:n.7998-212_7998-211delinsAC
ENST00000220616.8:c.7998-212_7998-211delinsAC	ENSP00000220616.4:n.7998-212_7998-211delinsAC
ENST00000519178.5:c.3364-212_3364-211delinsAC
ENST00000519543.5:c.2397-212_2397-211delinsAC	ENSP00000430430.1:n.2397-212_2397-211delinsAC
ENST00000521107.1:c.210-212_210-211delinsAC	ENSP00000430161.1:n.210-212_210-211delinsAC
ENST00000523756.5:c.4653-212_4653-211delinsAC
NM_003235.4:c.7998-212_7998-211delinsAC	NP_003226.4:n.7998-212_7998-211delinsAC
XM_005251038.3:c.7806-212_7806-211delinsAC	XP_005251095.1:n.7806-212_7806-211delinsAC
XM_006716622.2:c.7935-212_7935-211delinsAC	XP_006716685.1:n.7935-212_7935-211delinsAC
XM_005251038.4:c.7806-212_7806-211delinsAC	XP_005251095.1:n.7806-212_7806-211delinsAC
XM_006716622.3:c.7935-212_7935-211delinsAC	XP_006716685.1:n.7935-212_7935-211delinsAC
XM_017013793.1:c.7932-212_7932-211delinsAC	XP_016869282.1:n.7932-212_7932-211delinsAC
XM_017013794.1:c.7863-212_7863-211delinsAC	XP_016869283.1:n.7863-212_7863-211delinsAC
XM_017013795.1:c.7827-212_7827-211delinsAC	XP_016869284.1:n.7827-212_7827-211delinsAC
XM_017013796.1:c.7779-212_7779-211delinsAC	XP_016869285.1:n.7779-212_7779-211delinsAC
XM_017013797.1:c.7737-212_7737-211delinsAC	XP_016869286.1:n.7737-212_7737-211delinsAC
NM_003235.5:c.7998-212_7998-211delinsAC MANE Select	NP_003226.4:n.7998-212_7998-211delinsAC