Canonical Allele Identifier: CA354611177

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133495960A>C (hg19) ; chr3:g.133777116A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777116A>C , CM000665.2:g.133777116A>C	GRCh38
NC_000003.11:g.133495960A>C , CM000665.1:g.133495960A>C	GRCh37
NC_000003.10:g.134978650A>C	NCBI36
NG_013080.1:g.35984A>C
NG_013080.2:g.120119A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1940A>C MANE Select	ENSP00000385834.3:p.Asp647Ala
ENST00000402696.7:c.1940A>C	ENSP00000385834.3:p.Asp647Ala
ENST00000461695.1:c.671A>C
ENST00000467842.1:n.2934A>C
NM_001063.3:c.1940A>C	NP_001054.1:p.Asp647Ala
XM_011513100.1:c.1940A>C	XP_011511402.1:p.Asp647Ala
NM_001354703.1:c.1808A>C	NP_001341632.1:p.Asp603Ala
NM_001354704.1:c.1559A>C	NP_001341633.1:p.Asp520Ala
NM_001063.4:c.1940A>C MANE Select	NP_001054.2:p.Asp647Ala
NM_001354703.2:c.1808A>C	NP_001341632.2:p.Asp603Ala
NM_001354704.2:c.1559A>C	NP_001341633.2:p.Asp520Ala