Canonical Allele Identifier: CA354610391

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494369G>T (hg19) ; chr3:g.133775525G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775525G>T , CM000665.2:g.133775525G>T	GRCh38
NC_000003.11:g.133494369G>T , CM000665.1:g.133494369G>T	GRCh37
NC_000003.10:g.134977059G>T	NCBI36
NG_013080.1:g.34393G>T
NG_013080.2:g.118528G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1780G>T MANE Select	ENSP00000385834.3:p.Ala594Ser
ENST00000402696.7:c.1780G>T	ENSP00000385834.3:p.Ala594Ser
ENST00000461695.1:c.511G>T
ENST00000467842.1:n.2774G>T
NM_001063.3:c.1780G>T	NP_001054.1:p.Ala594Ser
XM_011513100.1:c.1780G>T	XP_011511402.1:p.Ala594Ser
NM_001354703.1:c.1648G>T	NP_001341632.1:p.Ala550Ser
NM_001354704.1:c.1399G>T	NP_001341633.1:p.Ala467Ser
NM_001063.4:c.1780G>T MANE Select	NP_001054.2:p.Ala594Ser
NM_001354703.2:c.1648G>T	NP_001341632.2:p.Ala550Ser
NM_001354704.2:c.1399G>T	NP_001341633.2:p.Ala467Ser