Canonical Allele Identifier: CA2739269003

Gene: TG

Linked Data

• ClinVar Variation Id: 2888457
• ClinVar RCV Id: RCV003724903

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132897728_132897729delinsTG , CM000670.2:g.132897728_132897729delinsTG	GRCh38
NC_000008.10:g.133909973_133909974delinsTG , CM000670.1:g.133909973_133909974delinsTG	GRCh37
NC_000008.9:g.133979155_133979156delinsTG	NCBI36
NG_015832.1:g.35769_35770delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.3081_3082delinsTG MANE Select	ENSP00000220616.4:p.Met1028Val
ENST00000220616.8:c.3081_3082delinsTG	ENSP00000220616.4:p.Met1028Val
ENST00000523756.5:c.40_41delinsTG
NM_003235.4:c.3081_3082delinsTG	NP_003226.4:p.Met1028Val
XM_005251038.3:c.3081_3082delinsTG	XP_005251095.1:p.Met1028Val
XM_005251040.3:c.3081_3082delinsTG	XP_005251097.1:p.Met1028Val
XM_005251042.3:c.3081_3082delinsTG	XP_005251099.1:p.Met1028Val
XM_005251043.3:c.3081_3082delinsTG	XP_005251100.1:p.Met1028Val
XM_006716622.2:c.3081_3082delinsTG	XP_006716685.1:p.Met1028Val
XM_005251038.4:c.3081_3082delinsTG	XP_005251095.1:p.Met1028Val
XM_005251040.4:c.3081_3082delinsTG	XP_005251097.1:p.Met1028Val
XM_005251042.4:c.3081_3082delinsTG	XP_005251099.1:p.Met1028Val
XM_006716622.3:c.3081_3082delinsTG	XP_006716685.1:p.Met1028Val
XM_017013793.1:c.3081_3082delinsTG	XP_016869282.1:p.Met1028Val
XM_017013794.1:c.3081_3082delinsTG	XP_016869283.1:p.Met1028Val
XM_017013795.1:c.3081_3082delinsTG	XP_016869284.1:p.Met1028Val
XM_017013796.1:c.3081_3082delinsTG	XP_016869285.1:p.Met1028Val
XM_017013797.1:c.2820_2821delinsTG	XP_016869286.1:p.Met941Val
XM_017013798.1:c.3081_3082delinsTG	XP_016869287.1:p.Met1028Val
XM_017013799.1:c.3081_3082delinsTG	XP_016869288.1:p.Met1028Val
XM_017013800.1:c.3081_3082delinsTG	XP_016869289.1:p.Met1028Val
NM_003235.5:c.3081_3082delinsTG MANE Select	NP_003226.4:p.Met1028Val