Canonical Allele Identifier: CA645516349

Gene: TF

Linked Data

• COSMIC: COSM1642095 ; COSM5347798

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775478_133775479del , CM000665.2:g.133775478_133775479del	GRCh38
NC_000003.11:g.133494322_133494323del , CM000665.1:g.133494322_133494323del	GRCh37
NC_000003.10:g.134977012_134977013del	NCBI36
NG_013080.1:g.34346_34347del
NG_013080.2:g.118481_118482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1733_1734del MANE Select	ENSP00000385834.3:p.Tyr578Ter
ENST00000402696.7:c.1733_1734del	ENSP00000385834.3:p.Tyr578Ter
ENST00000461695.1:c.464_465del
ENST00000467842.1:n.2727_2728del
NM_001063.3:c.1733_1734del	NP_001054.1:p.Tyr578Ter
XM_011513100.1:c.1733_1734del	XP_011511402.1:p.Tyr578Ter
NM_001354703.1:c.1601_1602del	NP_001341632.1:p.Tyr534Ter
NM_001354704.1:c.1352_1353del	NP_001341633.1:p.Tyr451Ter
NM_001063.4:c.1733_1734del MANE Select	NP_001054.2:p.Tyr578Ter
NM_001354703.2:c.1601_1602del	NP_001341632.2:p.Tyr534Ter
NM_001354704.2:c.1352_1353del	NP_001341633.2:p.Tyr451Ter