Canonical Allele Identifier: CA354608745

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133485231C>A (hg19) ; chr3:g.133766387C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766387C>A , CM000665.2:g.133766387C>A	GRCh38
NC_000003.11:g.133485231C>A , CM000665.1:g.133485231C>A	GRCh37
NC_000003.10:g.134967921C>A	NCBI36
NG_013080.1:g.25255C>A
NG_013080.2:g.109390C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1440C>A MANE Select	ENSP00000385834.3:p.Asn480Lys
ENST00000402696.7:c.1440C>A	ENSP00000385834.3:p.Asn480Lys
ENST00000461695.1:c.110C>A
NM_001063.3:c.1440C>A	NP_001054.1:p.Asn480Lys
XM_011513100.1:c.1440C>A	XP_011511402.1:p.Asn480Lys
NM_001354703.1:c.1308C>A	NP_001341632.1:p.Asn436Lys
NM_001354704.1:c.1059C>A	NP_001341633.1:p.Asn353Lys
NM_001063.4:c.1440C>A MANE Select	NP_001054.2:p.Asn480Lys
NM_001354703.2:c.1308C>A	NP_001341632.2:p.Asn436Lys
NM_001354704.2:c.1059C>A	NP_001341633.2:p.Asn353Lys