Canonical Allele Identifier: CA354610295

Gene: TF

Linked Data

• dbSNP Id: rs1934364258
• MyVariant Identifiers: chr3:g.133494328T>C (hg19) ; chr3:g.133775484T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775484T>C , CM000665.2:g.133775484T>C	GRCh38
NC_000003.11:g.133494328T>C , CM000665.1:g.133494328T>C	GRCh37
NC_000003.10:g.134977018T>C	NCBI36
NG_013080.1:g.34352T>C
NG_013080.2:g.118487T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1739T>C MANE Select	ENSP00000385834.3:p.Leu580Ser
ENST00000402696.7:c.1739T>C	ENSP00000385834.3:p.Leu580Ser
ENST00000461695.1:c.470T>C
ENST00000467842.1:n.2733T>C
NM_001063.3:c.1739T>C	NP_001054.1:p.Leu580Ser
XM_011513100.1:c.1739T>C	XP_011511402.1:p.Leu580Ser
NM_001354703.1:c.1607T>C	NP_001341632.1:p.Leu536Ser
NM_001354704.1:c.1358T>C	NP_001341633.1:p.Leu453Ser
NM_001063.4:c.1739T>C MANE Select	NP_001054.2:p.Leu580Ser
NM_001354703.2:c.1607T>C	NP_001341632.2:p.Leu536Ser
NM_001354704.2:c.1358T>C	NP_001341633.2:p.Leu453Ser