Canonical Allele Identifier: CA546290729

Gene: TF

Linked Data

• dbSNP Id: rs1426431071
• gnomAD v2: 3-133485099-CT-C
• gnomAD v4: 3-133766255-CT-C
• MyVariant Identifiers: chr3:g.133485100del (hg19) ; chr3:g.133766256del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766259del , CM000665.2:g.133766259del	GRCh38
NC_000003.11:g.133485103del , CM000665.1:g.133485103del	GRCh37
NC_000003.10:g.134967793del	NCBI36
NG_013080.1:g.25127del
NG_013080.2:g.109262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1331-19del MANE Select	ENSP00000385834.3:n.1331-19del
ENST00000402696.7:c.1331-19del	ENSP00000385834.3:n.1331-19del
NM_001063.3:c.1331-19del	NP_001054.1:n.1331-19del
XM_011513100.1:c.1331-19del	XP_011511402.1:n.1331-19del
NM_001354703.1:c.1199-19del	NP_001341632.1:n.1199-19del
NM_001354704.1:c.950-19del	NP_001341633.1:n.950-19del
NM_001063.4:c.1331-19del MANE Select	NP_001054.2:n.1331-19del
NM_001354703.2:c.1199-19del	NP_001341632.2:n.1199-19del
NM_001354704.2:c.950-19del	NP_001341633.2:n.950-19del