Canonical Allele Identifier: CA354604972

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475817G>T (hg19) ; chr3:g.133756973G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756973G>T , CM000665.2:g.133756973G>T	GRCh38
NC_000003.11:g.133475817G>T , CM000665.1:g.133475817G>T	GRCh37
NC_000003.10:g.134958507G>T	NCBI36
NG_013080.1:g.15841G>T
NG_013080.2:g.99976G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.834G>T MANE Select	ENSP00000385834.3:p.Lys278Asn
ENST00000402696.7:c.834G>T	ENSP00000385834.3:p.Lys278Asn
ENST00000485977.1:c.199G>T	ENSP00000418716.1:p.Gly67Ter
NM_001063.3:c.834G>T	NP_001054.1:p.Lys278Asn
XM_011513100.1:c.834G>T	XP_011511402.1:p.Lys278Asn
NM_001354703.1:c.702G>T	NP_001341632.1:p.Lys234Asn
NM_001354704.1:c.453G>T	NP_001341633.1:p.Lys151Asn
NM_001063.4:c.834G>T MANE Select	NP_001054.2:p.Lys278Asn
NM_001354703.2:c.702G>T	NP_001341632.2:p.Lys234Asn
NM_001354704.2:c.453G>T	NP_001341633.2:p.Lys151Asn