Canonical Allele Identifier: CA354605042

Gene: TF

Linked Data

• dbSNP Id: rs1289320184
• gnomAD v4: 3-133757004-G-T
• MyVariant Identifiers: chr3:g.133475848G>T (hg19) ; chr3:g.133757004G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757004G>T , CM000665.2:g.133757004G>T	GRCh38
NC_000003.11:g.133475848G>T , CM000665.1:g.133475848G>T	GRCh37
NC_000003.10:g.134958538G>T	NCBI36
NG_013080.1:g.15872G>T
NG_013080.2:g.100007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.865G>T MANE Select	ENSP00000385834.3:p.Ala289Ser
ENST00000402696.7:c.865G>T	ENSP00000385834.3:p.Ala289Ser
ENST00000485977.1:c.230G>T	ENSP00000418716.1:p.Gly77Val
NM_001063.3:c.865G>T	NP_001054.1:p.Ala289Ser
XM_011513100.1:c.865G>T	XP_011511402.1:p.Ala289Ser
NM_001354703.1:c.733G>T	NP_001341632.1:p.Ala245Ser
NM_001354704.1:c.484G>T	NP_001341633.1:p.Ala162Ser
NM_001063.4:c.865G>T MANE Select	NP_001054.2:p.Ala289Ser
NM_001354703.2:c.733G>T	NP_001341632.2:p.Ala245Ser
NM_001354704.2:c.484G>T	NP_001341633.2:p.Ala162Ser