Canonical Allele Identifier: CA2577907332

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766471T>C , CM000665.2:g.133766471T>C	GRCh38
NC_000003.11:g.133485315T>C , CM000665.1:g.133485315T>C	GRCh37
NC_000003.10:g.134968005T>C	NCBI36
NG_013080.1:g.25339T>C
NG_013080.2:g.109474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1486+38T>C MANE Select	ENSP00000385834.3:n.1486+38T>C
ENST00000402696.7:c.1486+38T>C	ENSP00000385834.3:n.1486+38T>C
ENST00000461695.1:c.156+38T>C
NM_001063.3:c.1486+38T>C	NP_001054.1:n.1486+38T>C
XM_011513100.1:c.1486+38T>C	XP_011511402.1:n.1486+38T>C
NM_001354703.1:c.1354+38T>C	NP_001341632.1:n.1354+38T>C
NM_001354704.1:c.1105+38T>C	NP_001341633.1:n.1105+38T>C
NM_001063.4:c.1486+38T>C MANE Select	NP_001054.2:n.1486+38T>C
NM_001354703.2:c.1354+38T>C	NP_001341632.2:n.1354+38T>C
NM_001354704.2:c.1105+38T>C	NP_001341633.2:n.1105+38T>C