Canonical Allele Identifier: CA2688665146

Gene: TG

Linked Data

• gnomAD v4: 8-133133275-CTTTGCAGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133276_133133284del , CM000670.2:g.133133276_133133284del	GRCh38
NC_000008.10:g.134145520_134145528del , CM000670.1:g.134145520_134145528del	GRCh37
NC_000008.9:g.134214702_134214710del	NCBI36
NG_015832.1:g.271316_271324del

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-194_7998-186del MANE Select	ENSP00000220616.4:n.7998-194_7998-186del
ENST00000220616.8:c.7998-194_7998-186del	ENSP00000220616.4:n.7998-194_7998-186del
ENST00000519178.5:c.3364-194_3364-186del
ENST00000519543.5:c.2397-194_2397-186del	ENSP00000430430.1:n.2397-194_2397-186del
ENST00000521107.1:c.210-194_210-186del	ENSP00000430161.1:n.210-194_210-186del
ENST00000523756.5:c.4653-194_4653-186del
NM_003235.4:c.7998-194_7998-186del	NP_003226.4:n.7998-194_7998-186del
XM_005251038.3:c.7806-194_7806-186del	XP_005251095.1:n.7806-194_7806-186del
XM_006716622.2:c.7935-194_7935-186del	XP_006716685.1:n.7935-194_7935-186del
XM_005251038.4:c.7806-194_7806-186del	XP_005251095.1:n.7806-194_7806-186del
XM_006716622.3:c.7935-194_7935-186del	XP_006716685.1:n.7935-194_7935-186del
XM_017013793.1:c.7932-194_7932-186del	XP_016869282.1:n.7932-194_7932-186del
XM_017013794.1:c.7863-194_7863-186del	XP_016869283.1:n.7863-194_7863-186del
XM_017013795.1:c.7827-194_7827-186del	XP_016869284.1:n.7827-194_7827-186del
XM_017013796.1:c.7779-194_7779-186del	XP_016869285.1:n.7779-194_7779-186del
XM_017013797.1:c.7737-194_7737-186del	XP_016869286.1:n.7737-194_7737-186del
NM_003235.5:c.7998-194_7998-186del MANE Select	NP_003226.4:n.7998-194_7998-186del