Canonical Allele Identifier: CA354611441

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133496037G>C (hg19) ; chr3:g.133777193G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777193G>C , CM000665.2:g.133777193G>C	GRCh38
NC_000003.11:g.133496037G>C , CM000665.1:g.133496037G>C	GRCh37
NC_000003.10:g.134978727G>C	NCBI36
NG_013080.1:g.36061G>C
NG_013080.2:g.120196G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.2017G>C MANE Select	ENSP00000385834.3:p.Glu673Gln
ENST00000402696.7:c.2017G>C	ENSP00000385834.3:p.Glu673Gln
ENST00000461695.1:c.748G>C
ENST00000467842.1:n.3011G>C
NM_001063.3:c.2017G>C	NP_001054.1:p.Glu673Gln
XM_011513100.1:c.2017G>C	XP_011511402.1:p.Glu673Gln
NM_001354703.1:c.1885G>C	NP_001341632.1:p.Glu629Gln
NM_001354704.1:c.1636G>C	NP_001341633.1:p.Glu546Gln
NM_001063.4:c.2017G>C MANE Select	NP_001054.2:p.Glu673Gln
NM_001354703.2:c.1885G>C	NP_001341632.2:p.Glu629Gln
NM_001354704.2:c.1636G>C	NP_001341633.2:p.Glu546Gln