Canonical Allele Identifier: CA2625042

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756262G>C , CM000665.2:g.133756262G>C	GRCh38
NC_000003.11:g.133475106G>C , CM000665.1:g.133475106G>C	GRCh37
NC_000003.10:g.134957796G>C	NCBI36
NG_013080.1:g.15130G>C
NG_013080.2:g.99265G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001063.4:c.636-20G>C MANE Select	NP_001054.2:n.636-20G>C
ENST00000402696.9:c.636-20G>C MANE Select	ENSP00000385834.3:n.636-20G>C
NM_001063.3:c.636-20G>C	NP_001054.1:n.636-20G>C
NM_001354703.1:c.504-20G>C	NP_001341632.1:n.504-20G>C
NM_001354703.2:c.504-20G>C	NP_001341632.2:n.504-20G>C
NM_001354704.1:c.255-20G>C	NP_001341633.1:n.255-20G>C
NM_001354704.2:c.255-20G>C	NP_001341633.2:n.255-20G>C
ENST00000402696.7:c.636-20G>C	ENSP00000385834.3:n.636-20G>C
ENST00000482271.5:c.255-20G>C	ENSP00000419338.1:n.255-20G>C
ENST00000485977.1:c.158-670G>C	ENSP00000418716.1:n.158-670G>C
XM_011513100.1:c.636-20G>C	XP_011511402.1:n.636-20G>C