Canonical Allele Identifier: CA1820984305

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873288_132873289delinsTG , CM000670.2:g.132873288_132873289delinsTG	GRCh38
NC_000008.10:g.133885533_133885534delinsTG , CM000670.1:g.133885533_133885534delinsTG	GRCh37
NC_000008.9:g.133954715_133954716delinsTG	NCBI36
NG_015832.1:g.11329_11330delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.638+67_638+68delinsTG MANE Select	ENSP00000220616.4:n.638+67_638+68delinsTG
ENST00000220616.8:c.638+67_638+68delinsTG	ENSP00000220616.4:n.638+67_638+68delinsTG
ENST00000523901.1:c.*489+67_*489+68delinsTG	ENSP00000427871.1:n.*489+67_*489+68delinsTG
NM_003235.4:c.638+67_638+68delinsTG	NP_003226.4:n.638+67_638+68delinsTG
XM_005251038.3:c.638+67_638+68delinsTG	XP_005251095.1:n.638+67_638+68delinsTG
XM_005251040.3:c.638+67_638+68delinsTG	XP_005251097.1:n.638+67_638+68delinsTG
XM_005251042.3:c.638+67_638+68delinsTG	XP_005251099.1:n.638+67_638+68delinsTG
XM_005251043.3:c.638+67_638+68delinsTG	XP_005251100.1:n.638+67_638+68delinsTG
XM_006716622.2:c.638+67_638+68delinsTG	XP_006716685.1:n.638+67_638+68delinsTG
XM_005251038.4:c.638+67_638+68delinsTG	XP_005251095.1:n.638+67_638+68delinsTG
XM_005251040.4:c.638+67_638+68delinsTG	XP_005251097.1:n.638+67_638+68delinsTG
XM_005251042.4:c.638+67_638+68delinsTG	XP_005251099.1:n.638+67_638+68delinsTG
XM_006716622.3:c.638+67_638+68delinsTG	XP_006716685.1:n.638+67_638+68delinsTG
XM_017013793.1:c.638+67_638+68delinsTG	XP_016869282.1:n.638+67_638+68delinsTG
XM_017013794.1:c.638+67_638+68delinsTG	XP_016869283.1:n.638+67_638+68delinsTG
XM_017013795.1:c.638+67_638+68delinsTG	XP_016869284.1:n.638+67_638+68delinsTG
XM_017013796.1:c.638+67_638+68delinsTG	XP_016869285.1:n.638+67_638+68delinsTG
XM_017013797.1:c.377+67_377+68delinsTG	XP_016869286.1:n.377+67_377+68delinsTG
XM_017013798.1:c.638+67_638+68delinsTG	XP_016869287.1:n.638+67_638+68delinsTG
XM_017013799.1:c.638+67_638+68delinsTG	XP_016869288.1:n.638+67_638+68delinsTG
XM_017013800.1:c.638+67_638+68delinsTG	XP_016869289.1:n.638+67_638+68delinsTG
NM_003235.5:c.638+67_638+68delinsTG MANE Select	NP_003226.4:n.638+67_638+68delinsTG