Canonical Allele Identifier: CA354604949

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475807T>A (hg19) ; chr3:g.133756963T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756963T>A , CM000665.2:g.133756963T>A	GRCh38
NC_000003.11:g.133475807T>A , CM000665.1:g.133475807T>A	GRCh37
NC_000003.10:g.134958497T>A	NCBI36
NG_013080.1:g.15831T>A
NG_013080.2:g.99966T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.824T>A MANE Select	ENSP00000385834.3:p.Met275Lys
ENST00000402696.7:c.824T>A	ENSP00000385834.3:p.Met275Lys
ENST00000485977.1:c.189T>A	ENSP00000418716.1:p.Tyr63Ter
NM_001063.3:c.824T>A	NP_001054.1:p.Met275Lys
XM_011513100.1:c.824T>A	XP_011511402.1:p.Met275Lys
NM_001354703.1:c.692T>A	NP_001341632.1:p.Met231Lys
NM_001354704.1:c.443T>A	NP_001341633.1:p.Met148Lys
NM_001063.4:c.824T>A MANE Select	NP_001054.2:p.Met275Lys
NM_001354703.2:c.692T>A	NP_001341632.2:p.Met231Lys
NM_001354704.2:c.443T>A	NP_001341633.2:p.Met148Lys