Canonical Allele Identifier: CA354604812

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475740C>G (hg19) ; chr3:g.133756896C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756896C>G , CM000665.2:g.133756896C>G	GRCh38
NC_000003.11:g.133475740C>G , CM000665.1:g.133475740C>G	GRCh37
NC_000003.10:g.134958430C>G	NCBI36
NG_013080.1:g.15764C>G
NG_013080.2:g.99899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.757C>G MANE Select	ENSP00000385834.3:p.Pro253Ala
ENST00000402696.7:c.757C>G	ENSP00000385834.3:p.Pro253Ala
ENST00000482271.5:c.376C>G	ENSP00000419338.1:p.Pro126Ala
ENST00000485977.1:c.158-36C>G	ENSP00000418716.1:n.158-36C>G
NM_001063.3:c.757C>G	NP_001054.1:p.Pro253Ala
XM_011513100.1:c.757C>G	XP_011511402.1:p.Pro253Ala
NM_001354703.1:c.625C>G	NP_001341632.1:p.Pro209Ala
NM_001354704.1:c.376C>G	NP_001341633.1:p.Pro126Ala
NM_001063.4:c.757C>G MANE Select	NP_001054.2:p.Pro253Ala
NM_001354703.2:c.625C>G	NP_001341632.2:p.Pro209Ala
NM_001354704.2:c.376C>G	NP_001341633.2:p.Pro126Ala