Canonical Allele Identifier: CA354611232
Gene: TF HGNC NCBI

Linked Data

dbSNP Id: rs1260597294

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133777128G>A , CM000665.2:g.133777128G>A GRCh38
NC_000003.11:g.133495972G>A , CM000665.1:g.133495972G>A GRCh37
NC_000003.10:g.134978662G>A NCBI36
NG_013080.1:g.35996G>A
NG_013080.2:g.120131G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1952G>A MANE Select ENSP00000385834.3:p.Arg651Lys
ENST00000402696.7:c.1952G>A ENSP00000385834.3:p.Arg651Lys
ENST00000461695.1:c.683G>A
ENST00000467842.1:n.2946G>A
NM_001063.3:c.1952G>A NP_001054.1:p.Arg651Lys
XM_011513100.1:c.1952G>A XP_011511402.1:p.Arg651Lys
NM_001354703.1:c.1820G>A NP_001341632.1:p.Arg607Lys
NM_001354704.1:c.1571G>A NP_001341633.1:p.Arg524Lys
NM_001063.4:c.1952G>A MANE Select NP_001054.2:p.Arg651Lys
NM_001354703.2:c.1820G>A NP_001341632.2:p.Arg607Lys
NM_001354704.2:c.1571G>A NP_001341633.2:p.Arg524Lys