Canonical Allele Identifier: CA505638393
Gene: KLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.12997913C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887099C>T , CM000681.2:g.12887099C>T GRCh38
NC_000019.9:g.12997913C>T , CM000681.1:g.12997913C>T GRCh37
NC_000019.8:g.12858913C>T NCBI36
NG_009292.1:g.940C>T
NG_013087.1:g.5105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.42G>A MANE Select ENSP00000264834.3:p.Leu14=
ENST00000264834.4:c.42G>A ENSP00000264834.3:p.Leu14=
NM_006563.3:c.42G>A NP_006554.1:p.Leu14=
XM_011527642.1:c.-162G>A XP_011525944.1:n.-162G>A
NM_006563.4:c.42G>A NP_006554.1:p.Leu14=
XM_011527642.2:c.-162G>A XP_011525944.1:n.-162G>A
NM_006563.5:c.42G>A MANE Select NP_006554.1:p.Leu14=