Canonical Allele Identifier: CA354604648

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475692G>C (hg19) ; chr3:g.133756848G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756848G>C , CM000665.2:g.133756848G>C	GRCh38
NC_000003.11:g.133475692G>C , CM000665.1:g.133475692G>C	GRCh37
NC_000003.10:g.134958382G>C	NCBI36
NG_013080.1:g.15716G>C
NG_013080.2:g.99851G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.709G>C MANE Select	ENSP00000385834.3:p.Ala237Pro
ENST00000402696.7:c.709G>C	ENSP00000385834.3:p.Ala237Pro
ENST00000482271.5:c.328G>C	ENSP00000419338.1:p.Ala110Pro
ENST00000485977.1:c.158-84G>C	ENSP00000418716.1:n.158-84G>C
NM_001063.3:c.709G>C	NP_001054.1:p.Ala237Pro
XM_011513100.1:c.709G>C	XP_011511402.1:p.Ala237Pro
NM_001354703.1:c.577G>C	NP_001341632.1:p.Ala193Pro
NM_001354704.1:c.328G>C	NP_001341633.1:p.Ala110Pro
NM_001063.4:c.709G>C MANE Select	NP_001054.2:p.Ala237Pro
NM_001354703.2:c.577G>C	NP_001341632.2:p.Ala193Pro
NM_001354704.2:c.328G>C	NP_001341633.2:p.Ala110Pro