Canonical Allele Identifier: CA9234047
Gene: KLF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328318
dbSNP Id: rs772655521

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12885752C>T , CM000681.2:g.12885752C>T GRCh38
NC_000019.9:g.12996566C>T , CM000681.1:g.12996566C>T GRCh37
NC_000019.8:g.12857566C>T NCBI36
NG_013087.1:g.6452G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.478G>A MANE Select ENSP00000264834.3:p.Glu160Lys
ENST00000264834.4:c.478G>A ENSP00000264834.3:p.Glu160Lys
NM_006563.3:c.478G>A NP_006554.1:p.Glu160Lys
XM_011527642.1:c.364G>A XP_011525944.1:p.Glu122Lys
NM_006563.4:c.478G>A NP_006554.1:p.Glu160Lys
XM_011527642.2:c.364G>A XP_011525944.1:p.Glu122Lys
NM_006563.5:c.478G>A MANE Select NP_006554.1:p.Glu160Lys