Canonical Allele Identifier: CA584913854

Gene: TG

Linked Data

• dbSNP Id: rs1462950446
• gnomAD v2: 8-133885299-A-ATTTTTTTT
• gnomAD v3: 8-132873054-A-ATTTTTTTT
• gnomAD v4: 8-132873054-A-ATTTTTTTT
• MyVariant Identifiers: chr8:g.133885299_133885300insTTTTTTTT (hg19) ; chr8:g.132873054_132873055insTTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873055_132873056insTTTTTTTT , CM000670.2:g.132873055_132873056insTTTTTTTT	GRCh38
NC_000008.10:g.133885300_133885301insTTTTTTTT , CM000670.1:g.133885300_133885301insTTTTTTTT	GRCh37
NC_000008.9:g.133954482_133954483insTTTTTTTT	NCBI36
NG_015832.1:g.11096_11097insTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.479-7_479-6insTTTTTTTT MANE Select	ENSP00000220616.4:n.479-7_479-6insTTTTTTTT
ENST00000220616.8:c.479-7_479-6insTTTTTTTT	ENSP00000220616.4:n.479-7_479-6insTTTTTTTT
ENST00000523901.1:c.*330-7_*330-6insTTTTTTTT	ENSP00000427871.1:n.*330-7_*330-6insTTTTTTTT
NM_003235.4:c.479-7_479-6insTTTTTTTT	NP_003226.4:n.479-7_479-6insTTTTTTTT
XM_005251038.3:c.479-7_479-6insTTTTTTTT	XP_005251095.1:n.479-7_479-6insTTTTTTTT
XM_005251040.3:c.479-7_479-6insTTTTTTTT	XP_005251097.1:n.479-7_479-6insTTTTTTTT
XM_005251042.3:c.479-7_479-6insTTTTTTTT	XP_005251099.1:n.479-7_479-6insTTTTTTTT
XM_005251043.3:c.479-7_479-6insTTTTTTTT	XP_005251100.1:n.479-7_479-6insTTTTTTTT
XM_006716622.2:c.479-7_479-6insTTTTTTTT	XP_006716685.1:n.479-7_479-6insTTTTTTTT
XM_005251038.4:c.479-7_479-6insTTTTTTTT	XP_005251095.1:n.479-7_479-6insTTTTTTTT
XM_005251040.4:c.479-7_479-6insTTTTTTTT	XP_005251097.1:n.479-7_479-6insTTTTTTTT
XM_005251042.4:c.479-7_479-6insTTTTTTTT	XP_005251099.1:n.479-7_479-6insTTTTTTTT
XM_006716622.3:c.479-7_479-6insTTTTTTTT	XP_006716685.1:n.479-7_479-6insTTTTTTTT
XM_017013793.1:c.479-7_479-6insTTTTTTTT	XP_016869282.1:n.479-7_479-6insTTTTTTTT
XM_017013794.1:c.479-7_479-6insTTTTTTTT	XP_016869283.1:n.479-7_479-6insTTTTTTTT
XM_017013795.1:c.479-7_479-6insTTTTTTTT	XP_016869284.1:n.479-7_479-6insTTTTTTTT
XM_017013796.1:c.479-7_479-6insTTTTTTTT	XP_016869285.1:n.479-7_479-6insTTTTTTTT
XM_017013797.1:c.218-7_218-6insTTTTTTTT	XP_016869286.1:n.218-7_218-6insTTTTTTTT
XM_017013798.1:c.479-7_479-6insTTTTTTTT	XP_016869287.1:n.479-7_479-6insTTTTTTTT
XM_017013799.1:c.479-7_479-6insTTTTTTTT	XP_016869288.1:n.479-7_479-6insTTTTTTTT
XM_017013800.1:c.479-7_479-6insTTTTTTTT	XP_016869289.1:n.479-7_479-6insTTTTTTTT
NM_003235.5:c.479-7_479-6insTTTTTTTT MANE Select	NP_003226.4:n.479-7_479-6insTTTTTTTT