Canonical Allele Identifier: CA2667772262

Gene: TF

Linked Data

• gnomAD v4: 3-133777033-T-TCTGTGAGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777037_133777038insGAGGTGCTGT , CM000665.2:g.133777037_133777038insGAGGTGCTGT	GRCh38
NC_000003.11:g.133495881_133495882insGAGGTGCTGT , CM000665.1:g.133495881_133495882insGAGGTGCTGT	GRCh37
NC_000003.10:g.134978571_134978572insGAGGTGCTGT	NCBI36
NG_013080.1:g.35905_35906insGAGGTGCTGT
NG_013080.2:g.120040_120041insGAGGTGCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-12_1873-11insGAGGTGCTGT MANE Select	ENSP00000385834.3:n.1873-12_1873-11insGAG...
ENST00000402696.7:c.1873-12_1873-11insGAGGTGCTGT	ENSP00000385834.3:n.1873-12_1873-11insGAG...
ENST00000461695.1:c.604-12_604-11insGAGGTGCTGT
ENST00000467842.1:n.2867-12_2867-11insGAGGTGCTGT
NM_001063.3:c.1873-12_1873-11insGAGGTGCTGT	NP_001054.1:n.1873-12_1873-11insGAGGTGCTG...
XM_011513100.1:c.1873-12_1873-11insGAGGTGCTGT	XP_011511402.1:n.1873-12_1873-11insGAGGTG...
NM_001354703.1:c.1741-12_1741-11insGAGGTGCTGT	NP_001341632.1:n.1741-12_1741-11insGAGGTG...
NM_001354704.1:c.1492-12_1492-11insGAGGTGCTGT	NP_001341633.1:n.1492-12_1492-11insGAGGTG...
NM_001063.4:c.1873-12_1873-11insGAGGTGCTGT MANE Select	NP_001054.2:n.1873-12_1873-11insGAGGTGCTG...
NM_001354703.2:c.1741-12_1741-11insGAGGTGCTGT	NP_001341632.2:n.1741-12_1741-11insGAGGTG...
NM_001354704.2:c.1492-12_1492-11insGAGGTGCTGT	NP_001341633.2:n.1492-12_1492-11insGAGGTG...