Canonical Allele Identifier: CA2688665135

Gene: TG

Linked Data

• gnomAD v4: 8-133133266-ATGGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133268_133133272del , CM000670.2:g.133133268_133133272del	GRCh38
NC_000008.10:g.134145512_134145516del , CM000670.1:g.134145512_134145516del	GRCh37
NC_000008.9:g.134214694_134214698del	NCBI36
NG_015832.1:g.271308_271312del

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-202_7998-198del MANE Select	ENSP00000220616.4:n.7998-202_7998-198del
ENST00000220616.8:c.7998-202_7998-198del	ENSP00000220616.4:n.7998-202_7998-198del
ENST00000519178.5:c.3364-202_3364-198del
ENST00000519543.5:c.2397-202_2397-198del	ENSP00000430430.1:n.2397-202_2397-198del
ENST00000521107.1:c.210-202_210-198del	ENSP00000430161.1:n.210-202_210-198del
ENST00000523756.5:c.4653-202_4653-198del
NM_003235.4:c.7998-202_7998-198del	NP_003226.4:n.7998-202_7998-198del
XM_005251038.3:c.7806-202_7806-198del	XP_005251095.1:n.7806-202_7806-198del
XM_006716622.2:c.7935-202_7935-198del	XP_006716685.1:n.7935-202_7935-198del
XM_005251038.4:c.7806-202_7806-198del	XP_005251095.1:n.7806-202_7806-198del
XM_006716622.3:c.7935-202_7935-198del	XP_006716685.1:n.7935-202_7935-198del
XM_017013793.1:c.7932-202_7932-198del	XP_016869282.1:n.7932-202_7932-198del
XM_017013794.1:c.7863-202_7863-198del	XP_016869283.1:n.7863-202_7863-198del
XM_017013795.1:c.7827-202_7827-198del	XP_016869284.1:n.7827-202_7827-198del
XM_017013796.1:c.7779-202_7779-198del	XP_016869285.1:n.7779-202_7779-198del
XM_017013797.1:c.7737-202_7737-198del	XP_016869286.1:n.7737-202_7737-198del
NM_003235.5:c.7998-202_7998-198del MANE Select	NP_003226.4:n.7998-202_7998-198del