Canonical Allele Identifier: CA847740783

Gene: TG

Linked Data

• dbSNP Id: rs1176811887
• gnomAD v3: 8-133133270-CCTAGCTTTGCAGTG-C
• gnomAD v4: 8-133133270-CCTAGCTTTGCAGTG-C
• MyVariant Identifiers: chr8:g.134145515_134145528del (hg19) ; chr8:g.133133271_133133284del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133286_133133299del , CM000670.2:g.133133286_133133299del	GRCh38
NC_000008.10:g.134145530_134145543del , CM000670.1:g.134145530_134145543del	GRCh37
NC_000008.9:g.134214712_134214725del	NCBI36
NG_015832.1:g.271326_271339del

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-184_7998-171del MANE Select	ENSP00000220616.4:n.7998-184_7998-171del
ENST00000220616.8:c.7998-184_7998-171del	ENSP00000220616.4:n.7998-184_7998-171del
ENST00000519178.5:c.3364-184_3364-171del
ENST00000519543.5:c.2397-184_2397-171del	ENSP00000430430.1:n.2397-184_2397-171del
ENST00000521107.1:c.210-184_210-171del	ENSP00000430161.1:n.210-184_210-171del
ENST00000523756.5:c.4653-184_4653-171del
NM_003235.4:c.7998-184_7998-171del	NP_003226.4:n.7998-184_7998-171del
XM_005251038.3:c.7806-184_7806-171del	XP_005251095.1:n.7806-184_7806-171del
XM_006716622.2:c.7935-184_7935-171del	XP_006716685.1:n.7935-184_7935-171del
XM_005251038.4:c.7806-184_7806-171del	XP_005251095.1:n.7806-184_7806-171del
XM_006716622.3:c.7935-184_7935-171del	XP_006716685.1:n.7935-184_7935-171del
XM_017013793.1:c.7932-184_7932-171del	XP_016869282.1:n.7932-184_7932-171del
XM_017013794.1:c.7863-184_7863-171del	XP_016869283.1:n.7863-184_7863-171del
XM_017013795.1:c.7827-184_7827-171del	XP_016869284.1:n.7827-184_7827-171del
XM_017013796.1:c.7779-184_7779-171del	XP_016869285.1:n.7779-184_7779-171del
XM_017013797.1:c.7737-184_7737-171del	XP_016869286.1:n.7737-184_7737-171del
NM_003235.5:c.7998-184_7998-171del MANE Select	NP_003226.4:n.7998-184_7998-171del