Canonical Allele Identifier: CA1820984204

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873046_132873054delinsTCGTGAAAA , CM000670.2:g.132873046_132873054delinsTCGTGAAAA	GRCh38
NC_000008.10:g.133885291_133885299delinsTCGTGAAAA , CM000670.1:g.133885291_133885299delinsTCGTGAAAA	GRCh37
NC_000008.9:g.133954473_133954481delinsTCGTGAAAA	NCBI36
NG_015832.1:g.11087_11095delinsTCGTGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.479-16_479-8delinsTCGTGAAAA MANE Select	ENSP00000220616.4:n.479-16_479-8delinsTCGTGAAAA
ENST00000220616.8:c.479-16_479-8delinsTCGTGAAAA	ENSP00000220616.4:n.479-16_479-8delinsTCGTGAAAA
ENST00000523901.1:c.*330-16_*330-8delinsTCGTGAAAA	ENSP00000427871.1:n.*330-16_*330-8delinsTCGTGAAAA
NM_003235.4:c.479-16_479-8delinsTCGTGAAAA	NP_003226.4:n.479-16_479-8delinsTCGTGAAAA
XM_005251038.3:c.479-16_479-8delinsTCGTGAAAA	XP_005251095.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251040.3:c.479-16_479-8delinsTCGTGAAAA	XP_005251097.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251042.3:c.479-16_479-8delinsTCGTGAAAA	XP_005251099.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251043.3:c.479-16_479-8delinsTCGTGAAAA	XP_005251100.1:n.479-16_479-8delinsTCGTGAAAA
XM_006716622.2:c.479-16_479-8delinsTCGTGAAAA	XP_006716685.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251038.4:c.479-16_479-8delinsTCGTGAAAA	XP_005251095.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251040.4:c.479-16_479-8delinsTCGTGAAAA	XP_005251097.1:n.479-16_479-8delinsTCGTGAAAA
XM_005251042.4:c.479-16_479-8delinsTCGTGAAAA	XP_005251099.1:n.479-16_479-8delinsTCGTGAAAA
XM_006716622.3:c.479-16_479-8delinsTCGTGAAAA	XP_006716685.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013793.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869282.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013794.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869283.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013795.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869284.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013796.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869285.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013797.1:c.218-16_218-8delinsTCGTGAAAA	XP_016869286.1:n.218-16_218-8delinsTCGTGAAAA
XM_017013798.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869287.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013799.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869288.1:n.479-16_479-8delinsTCGTGAAAA
XM_017013800.1:c.479-16_479-8delinsTCGTGAAAA	XP_016869289.1:n.479-16_479-8delinsTCGTGAAAA
NM_003235.5:c.479-16_479-8delinsTCGTGAAAA MANE Select	NP_003226.4:n.479-16_479-8delinsTCGTGAAAA