Canonical Allele Identifier: CA4885916

Gene: TG

Linked Data

• dbSNP Id: rs754396483
• ExAC: 8:134145904 GGT / G
• gnomAD v2: 8-134145904-GGT-G
• gnomAD v4: 8-133133660-GGT-G
• MyVariant Identifiers: chr8:g.134145905_134145906del (hg19) ; chr8:g.133133661_133133662del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133661_133133662del , CM000670.2:g.133133661_133133662del	GRCh38
NC_000008.10:g.134145905_134145906del , CM000670.1:g.134145905_134145906del	GRCh37
NC_000008.9:g.134215087_134215088del	NCBI36
NG_015832.1:g.271701_271702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+1_8188+2del MANE Select	ENSP00000220616.4:n.8188+1_8188+2del
ENST00000220616.8:c.8188+1_8188+2del	ENSP00000220616.4:n.8188+1_8188+2del
ENST00000519178.5:c.3554+1_3554+2del
ENST00000519543.5:c.2587+1_2587+2del	ENSP00000430430.1:n.2587+1_2587+2del
ENST00000521107.1:c.400+1_400+2del	ENSP00000430161.1:n.400+1_400+2del
ENST00000522691.1:n.274+1_274+2del
ENST00000523756.5:c.4843+1_4843+2del
NM_003235.4:c.8188+1_8188+2del	NP_003226.4:n.8188+1_8188+2del
XM_005251038.3:c.7996+1_7996+2del	XP_005251095.1:n.7996+1_7996+2del
XM_006716622.2:c.8125+1_8125+2del	XP_006716685.1:n.8125+1_8125+2del
XM_005251038.4:c.7996+1_7996+2del	XP_005251095.1:n.7996+1_7996+2del
XM_006716622.3:c.8125+1_8125+2del	XP_006716685.1:n.8125+1_8125+2del
XM_017013793.1:c.8122+1_8122+2del	XP_016869282.1:n.8122+1_8122+2del
XM_017013794.1:c.8053+1_8053+2del	XP_016869283.1:n.8053+1_8053+2del
XM_017013795.1:c.8017+1_8017+2del	XP_016869284.1:n.8017+1_8017+2del
XM_017013796.1:c.7969+1_7969+2del	XP_016869285.1:n.7969+1_7969+2del
XM_017013797.1:c.7927+1_7927+2del	XP_016869286.1:n.7927+1_7927+2del
NM_003235.5:c.8188+1_8188+2del MANE Select	NP_003226.4:n.8188+1_8188+2del