Canonical Allele Identifier: CA435815811

Gene: TF

Linked Data

• COSMIC: COSM4900528
• MyVariant Identifiers: chr3:g.133494306C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775462C>T , CM000665.2:g.133775462C>T	GRCh38
NC_000003.11:g.133494306C>T , CM000665.1:g.133494306C>T	GRCh37
NC_000003.10:g.134976996C>T	NCBI36
NG_013080.1:g.34330C>T
NG_013080.2:g.118465C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1717C>T MANE Select	ENSP00000385834.3:p.Leu573=
ENST00000402696.7:c.1717C>T	ENSP00000385834.3:p.Leu573=
ENST00000461695.1:c.448C>T
ENST00000467842.1:n.2711C>T
NM_001063.3:c.1717C>T	NP_001054.1:p.Leu573=
XM_011513100.1:c.1717C>T	XP_011511402.1:p.Leu573=
NM_001354703.1:c.1585C>T	NP_001341632.1:p.Leu529=
NM_001354704.1:c.1336C>T	NP_001341633.1:p.Leu446=
NM_001063.4:c.1717C>T MANE Select	NP_001054.2:p.Leu573=
NM_001354703.2:c.1585C>T	NP_001341632.2:p.Leu529=
NM_001354704.2:c.1336C>T	NP_001341633.2:p.Leu446=