Canonical Allele Identifier: CA2667764515

Gene: TF

Linked Data

• gnomAD v4: 3-133757004-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757007del , CM000665.2:g.133757007del	GRCh38
NC_000003.11:g.133475851del , CM000665.1:g.133475851del	GRCh37
NC_000003.10:g.134958541del	NCBI36
NG_013080.1:g.15875del
NG_013080.2:g.100010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.868del MANE Select	ENSP00000385834.3:p.Gln290ArgfsTer?
ENST00000402696.7:c.868del	ENSP00000385834.3:p.Gln290ArgfsTer?
ENST00000485977.1:c.233del	ENSP00000418716.1:p.Pro78GlnfsTer?
NM_001063.3:c.868del	NP_001054.1:p.Gln290ArgfsTer?
XM_011513100.1:c.868del	XP_011511402.1:p.Gln290ArgfsTer?
NM_001354703.1:c.736del	NP_001341632.1:p.Gln246ArgfsTer?
NM_001354704.1:c.487del	NP_001341633.1:p.Gln163ArgfsTer?
NM_001063.4:c.868del MANE Select	NP_001054.2:p.Gln290ArgfsTer?
NM_001354703.2:c.736del	NP_001341632.2:p.Gln246ArgfsTer?
NM_001354704.2:c.487del	NP_001341633.2:p.Gln163ArgfsTer?