Canonical Allele Identifier: CA9234067
Gene: KLF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328322
ClinVar RCV Id: RCV000391619
dbSNP Id: rs748056490

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12885944G>A , CM000681.2:g.12885944G>A GRCh38
NC_000019.9:g.12996758G>A , CM000681.1:g.12996758G>A GRCh37
NC_000019.8:g.12857758G>A NCBI36
NG_013087.1:g.6260C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.286C>T MANE Select ENSP00000264834.3:p.Leu96=
ENST00000264834.4:c.286C>T ENSP00000264834.3:p.Leu96=
NM_006563.3:c.286C>T NP_006554.1:p.Leu96=
XM_011527642.1:c.172C>T XP_011525944.1:p.Leu58=
NM_006563.4:c.286C>T NP_006554.1:p.Leu96=
XM_011527642.2:c.172C>T XP_011525944.1:p.Leu58=
NM_006563.5:c.286C>T MANE Select NP_006554.1:p.Leu96=