Canonical Allele Identifier: CA4885867

Gene: TG

Linked Data

• dbSNP Id: rs761032421
• ExAC: 8:134145672 CAA / C
• gnomAD v2: 8-134145672-CAA-C
• gnomAD v3: 8-133133428-CAA-C
• gnomAD v4: 8-133133428-CAA-C
• MyVariant Identifiers: chr8:g.134145673_134145674del (hg19) ; chr8:g.133133429_133133430del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133430_133133431del , CM000670.2:g.133133430_133133431del	GRCh38
NC_000008.10:g.134145674_134145675del , CM000670.1:g.134145674_134145675del	GRCh37
NC_000008.9:g.134214856_134214857del	NCBI36
NG_015832.1:g.271470_271471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-40_7998-39del MANE Select	ENSP00000220616.4:n.7998-40_7998-39del
ENST00000220616.8:c.7998-40_7998-39del	ENSP00000220616.4:n.7998-40_7998-39del
ENST00000519178.5:c.3364-40_3364-39del
ENST00000519543.5:c.2397-40_2397-39del	ENSP00000430430.1:n.2397-40_2397-39del
ENST00000521107.1:c.210-40_210-39del	ENSP00000430161.1:n.210-40_210-39del
ENST00000522691.1:n.44_45del
ENST00000523756.5:c.4653-40_4653-39del
NM_003235.4:c.7998-40_7998-39del	NP_003226.4:n.7998-40_7998-39del
XM_005251038.3:c.7806-40_7806-39del	XP_005251095.1:n.7806-40_7806-39del
XM_006716622.2:c.7935-40_7935-39del	XP_006716685.1:n.7935-40_7935-39del
XM_005251038.4:c.7806-40_7806-39del	XP_005251095.1:n.7806-40_7806-39del
XM_006716622.3:c.7935-40_7935-39del	XP_006716685.1:n.7935-40_7935-39del
XM_017013793.1:c.7932-40_7932-39del	XP_016869282.1:n.7932-40_7932-39del
XM_017013794.1:c.7863-40_7863-39del	XP_016869283.1:n.7863-40_7863-39del
XM_017013795.1:c.7827-40_7827-39del	XP_016869284.1:n.7827-40_7827-39del
XM_017013796.1:c.7779-40_7779-39del	XP_016869285.1:n.7779-40_7779-39del
XM_017013797.1:c.7737-40_7737-39del	XP_016869286.1:n.7737-40_7737-39del
NM_003235.5:c.7998-40_7998-39del MANE Select	NP_003226.4:n.7998-40_7998-39del