Canonical Allele Identifier: CA354610338

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494346C>G (hg19) ; chr3:g.133775502C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775502C>G , CM000665.2:g.133775502C>G	GRCh38
NC_000003.11:g.133494346C>G , CM000665.1:g.133494346C>G	GRCh37
NC_000003.10:g.134977036C>G	NCBI36
NG_013080.1:g.34370C>G
NG_013080.2:g.118505C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1757C>G MANE Select	ENSP00000385834.3:p.Thr586Ser
ENST00000402696.7:c.1757C>G	ENSP00000385834.3:p.Thr586Ser
ENST00000461695.1:c.488C>G
ENST00000467842.1:n.2751C>G
NM_001063.3:c.1757C>G	NP_001054.1:p.Thr586Ser
XM_011513100.1:c.1757C>G	XP_011511402.1:p.Thr586Ser
NM_001354703.1:c.1625C>G	NP_001341632.1:p.Thr542Ser
NM_001354704.1:c.1376C>G	NP_001341633.1:p.Thr459Ser
NM_001063.4:c.1757C>G MANE Select	NP_001054.2:p.Thr586Ser
NM_001354703.2:c.1625C>G	NP_001341632.2:p.Thr542Ser
NM_001354704.2:c.1376C>G	NP_001341633.2:p.Thr459Ser