Canonical Allele Identifier: CA354611166

Gene: TF

Linked Data

• COSMIC: COSM3122418
• MyVariant Identifiers: chr3:g.133495959G>A (hg19) ; chr3:g.133777115G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777115G>A , CM000665.2:g.133777115G>A	GRCh38
NC_000003.11:g.133495959G>A , CM000665.1:g.133495959G>A	GRCh37
NC_000003.10:g.134978649G>A	NCBI36
NG_013080.1:g.35983G>A
NG_013080.2:g.120118G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1939G>A MANE Select	ENSP00000385834.3:p.Asp647Asn
ENST00000402696.7:c.1939G>A	ENSP00000385834.3:p.Asp647Asn
ENST00000461695.1:c.670G>A
ENST00000467842.1:n.2933G>A
NM_001063.3:c.1939G>A	NP_001054.1:p.Asp647Asn
XM_011513100.1:c.1939G>A	XP_011511402.1:p.Asp647Asn
NM_001354703.1:c.1807G>A	NP_001341632.1:p.Asp603Asn
NM_001354704.1:c.1558G>A	NP_001341633.1:p.Asp520Asn
NM_001063.4:c.1939G>A MANE Select	NP_001054.2:p.Asp647Asn
NM_001354703.2:c.1807G>A	NP_001341632.2:p.Asp603Asn
NM_001354704.2:c.1558G>A	NP_001341633.2:p.Asp520Asn